DIN EN ISO 11953:2010-11
|
Dentistry - Implants - Clinical performance of hand torque instruments (ISO 11953:2010), German version EN ISO 11953:2010 |
DIN EN ISO 21672-1:2012-07
|
Dentistry - Periodontal probes - Part 1: General requirements (ISO 21672-1:2012) |
I.S. EN 1041:2008+A1:2013
|
INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
I.S. EN ISO 11953:2010
|
DENTISTRY - IMPLANTS - CLINICAL PERFORMANCE OF HAND TORQUE INSTRUMENTS |
NF EN 80601-2-58:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
14/30261090 DC : 0
|
BS EN ISO 17937 - DENTISTRY - OSTEOTOME FOR BONE COMPACTION AND SINUS FLOOR ELEVATION |
DIN EN ISO 3630-4:2009-10
|
Dentistry - Root canal instruments - Part 4: Auxiliary instruments (ISO 3630-4:2009) |
BS EN ISO 13504:2012
|
Dentistry. General requirements for instruments and related accessories used in dental implant placement and treatment |
I.S. EN 15424:2007
|
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
15/30328959 DC : 0
|
BS ISO 16142-2 - MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 2: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
12/30261215 DC : 0
|
BS EN 13060 - SMALL STEAM STERILIZERS |
BS EN ISO 80601-2-56:2017
|
Medical electrical equipment Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement |
BS EN ISO 21672-1:2012
|
Dentistry. Periodontal probes General requirements |
09/30203808 DC : 0
|
BS EN ISO 80601-2-12 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
16/30310674 DC : 0
|
BS EN ISO 14457 - DENTISTRY - HANDPIECES AND MOTORS |
16/30297742 DC : DRAFT JUNE 2016
|
BS EN ISO 19490 - DENTISTRY - SINUS MEMBRANE ELEVATOR |
DIN EN ISO 16061:2015-09
|
Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
I.S. EN ISO 18397:2016
|
DENTISTRY - POWERED SCALER (ISO 18397:2016) |
DD CEN ISO/TS 11135-2:2008
|
Sterilization of health care products. Ethylene oxide Guidance on the application of ISO 11135-1 |
UNE-EN ISO 19490:2018
|
Dentistry - Sinus membrane elevator (ISO 19490:2017) |
DIN EN ISO 80601-2-69 E : 2014
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-69: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF OXYGEN CONCENTRATOR EQUIPMENT (ISO 80601-2-69:2014) |
15/30314608 DC : 0
|
BS EN ISO 7153-1 - SURGICAL INSTRUMENTS - MATERIALS - PART 1: METALS |
16/30302541 DC : 0
|
BS EN ISO 19715 - DENTISTRY - FILLING INSTRUMENTS WITH CONTRA SET |
15/30297745 DC : 0
|
BS EN ISO 9173-1 - DENTISTRY - EXTRACTION FORCEPS - PART 1: GENERAL REQUIREMENTS |
10/30205392 DC : 0
|
BS ISO 7494-1 - DENTISTRY - DENTAL UNITS - PART 1: GENERAL REQUIREMENTS AND TEST METHODS |
DIN EN ISO 11135:2014-10
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11135:2014) |
15/30312454 DC : 0
|
BS EN ISO 80601-2-56 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-56: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CLINICAL THERMOMETERS FOR BODY TEMPERATURE MEASUREMENT |
CSA Z10651-5 : 2008 : R2013
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
07/30157980 DC : 0
|
BS EN 60601-2-58 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
CSA Z11135-2 : 2009 : FR
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
CSA Z17665-2 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
04/30088362 DC : DRAFT NOV 2004
|
ISO 10651-5 - LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY VENTILATORS |
CAN/CSA-C22.2 NO. 80601-2-67:17
|
Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen conserving equipment (Adopted ISO 80601-2-67:2014, first edition, 2014-06-01, with Canadian deviations) |
CSA ISO 14937 : 2011
|
STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
DIN EN ISO 11135-1:2007-08
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
CSA Z10651-5 : 2008 : INC : UPD 1 : 2011
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
PREN 13060 : DRAFT 2012
|
SMALL STEAM STERILIZERS |
DIN EN ISO 18397:2016-09
|
DENTISTRY - POWERED SCALER (ISO 18397:2016) |
ANSI/AAMI/ISO 14937:2009(R2013)
|
STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNE-EN ISO 80601-2-69:2015
|
Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014) |
AAMI/ISO TIR17665-3:2014(R2016)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - GUIDANCE ON THE DESIGNATION OF A MEDICAL PRODUCT TO A PRODUCT FAMILY AND PROCESSING CATEGORY FOR STEAM STERILIZATION |
ANSI/AAMI/ISO 11135:2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
BS EN ISO 80601-2-12:2011
|
Medical electrical equipment Particular requirements for basic safety and essential performance of critical care ventilators |
CSA C22.2 No. 80601-2-55 : 2014(R2019)
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
I.S. EN ISO 21672-1:2012
|
DENTISTRY - PERIODONTAL PROBES - PART 1: GENERAL REQUIREMENTS (ISO 21672-1:2012) |
I.S. EN 15546-1:2008
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
I.S. EN ISO 18556:2016
|
DENTISTRY - INTRAORAL SPATULAS (ISO 18556:2016) |
ISO 16142-1:2016
|
Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
CSA Z17665-1 : 2009 : FR
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNE-EN ISO 22442-1:2016
|
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) |
UNI EN ISO 7494-1 : 2011
|
DENTISTRY - DENTAL UNITS - PART 1: GENERAL REQUIREMENTS AND TEST METHODS |
UNE-EN ISO 16635-2:2015
|
Dentistry - Dental rubber dam instruments - Part 2: Clamp forceps(ISO 16635-2:2014) |
ISO 80601-2-74:2017
|
Medical electrical equipment Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment |
DIN EN ISO 22442-1:2016-05
|
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) |
DIN EN ISO 15883-2:2009-09
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANAESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
ISO 15883-2:2006
|
Washer-disinfectors Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc. |
ISO 11135-1:2007
|
Sterilization of health care products Ethylene oxide Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices |
BS EN ISO 7153-1:2016
|
Surgical instruments. Materials Metals |
BS EN 15424:2007
|
Sterilization of medical devices. Low temperature steam and formaldehyde. Requirements for development, validation and routine control of a sterilization process for medical devices |
BS EN ISO 14630:2012
|
Non-active surgical implants. General requirements |
CEN ISO/TS 11135-2:2008/AC:2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
EN 80601-2-58:2015
|
Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
DIN EN 15424:2007-08
|
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
VDI 5700 Blatt 1:2015-04
|
Reprocessing hazards - Risk management in reprocessing of medical devices - Measures for risk control |
BS ISO 19611:2017
|
Traditional Chinese medicine. Air extraction cupping device |
UNI EN ISO 16635-2 : 2014
|
DENTISTRY - DENTAL RUBBER DAM INSTRUMENTS - PART 2: CLAMP FORCEPS |
BS EN ISO 16635-2:2014
|
Dentistry. Dental rubber dam instruments Clamp forceps |
12/30245297 DC : 0
|
BS EN ISO 16635-2 - DENTISTRY - RUBBER DAM TECHNIQUE - PART 2: RUBBER DAM CLAMP FORCEPS |
BS EN ISO 20857:2013
|
Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of a sterilization process for medical devices |
BS EN ISO 80601-2-72:2015
|
Medical electrical equipment Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients |
DIN EN ISO 9168:2009-10
|
DENTISTRY - HOSE CONNECTORS FOR AIR DRIVEN DENTAL HANDPIECES |
UNE-EN ISO 16061:2015
|
Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
15/30278527 DC : 0
|
BS EN ISO 18559 - DENTISTRY - EXTRAORAL SPATULAS FOR MIXING DENTAL CEMENTS |
UNE-EN ISO 13504:2013
|
Dentistry - General requirements for instruments and related accessories used in dental implant placement and treatment (ISO 13504:2012) |
BS EN ISO 19490:2017
|
Dentistry. Sinus membrane elevator |
DIN EN 15546-1:2008-08
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
DIN EN ISO 80601-2-72:2016-04
|
Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (ISO 80601-2-72:2015) |
BS EN ISO 19715:2017
|
Dentistry. Filling instrument with contra angle |
PD ISO/TS 17665-3:2013
|
Sterilization of health care products. Moist heat Guidance on the designation of a medical device to a product family and processing category for steam sterilization |
ISO 20308:2017
|
Traditional Chinese medicine — Gua Sha instruments |
16/30312315 DC : 0
|
BS EN ISO 80601-2-55 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
11/30212235 DC : 0
|
BS EN ISO 13504 - DENTISTRY - GENERAL REQUIREMENTS FOR INSTRUMENTS AND RELATED ACCESSORIES USED IN DENTAL IMPLANT PLACEMENT AND TREATMENT |
UNI EN ISO 80601-2-12 : 2011
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
11/30212226 DC : 0
|
BS ISO 21672-1 - DENTISTRY - PERIODONTAL PROBES - PART 1: GENERAL REQUIREMENTS |
DIN EN ISO 17937:2016-01
|
Dentistry - Osteotome (ISO 17937:2015) |
DIN EN ISO 9168 E : 2009
|
DENTISTRY - HOSE CONNECTORS FOR AIR DRIVEN DENTAL HANDPIECES |
DIN EN ISO 22374:2005-12
|
DENTISTRY - DENTAL HANDPIECES - ELECTRICAL-POWERED SCALERS AND SCALER TIPS |
NF CEN ISO/TS 11135-2 : 2008
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
04/30048205 DC : DRAFT JUL 2004
|
BS EN ISO 17665 - STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
09/30180393 DC : 0
|
BS EN ISO 10451 - DENTISTRY - CONTENTS OF TECHNICAL FILE FOR DENTAL IMPLANT SYSTEMS |
UNE-EN ISO 18556:2016
|
Dentistry - Intraoral spatulas (ISO 18556:2016) |
CSA ISO 27427 : 2014
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - NEBULIZING SYSTEMS AND COMPONENTS |
16/30302520 DC : 0
|
BS ISO 19611 - TRADITIONAL CHINESE MEDICINE - AIR EXHAUST CUPPING APPARATUS FOR MEDICAL USE |
I.S. EN ISO 80601-2-56:2017
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-56: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CLINICAL THERMOMETERS FOR BODY TEMPERATURE MEASUREMENT (ISO 80601-2-56:2017) |
CSA Z10651-5 : 2008
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
AAMI ISO 17665-1 : 2006
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
I.S. EN ISO 17937:2015
|
DENTISTRY - OSTEOTOME (ISO 17937:2015) |
ANSI/AAMI/ISO 20857:2010(R2015)
|
STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNI CEN ISO/TS 17665-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
ISO 19979:2018
|
Ophthalmic optics — Contact lenses — Hygienic management of multipatient use trial contact lenses |
I.S. EN 80601-2-60:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-60: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF DENTAL EQUIPMENT |
ISO 5910:2018
|
Cardiovascular implants and extracorporeal systems Cardiac valve repair devices |
CAN/CSA-C22.2 NO. 80601-2-72:17
|
Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (Adopted ISO 80601-2-72:2015, first edition, 2015-09-01, with Canadian deviations) |
ISO 8828:2014
|
Implants for surgery Guidance on care and handling of orthopaedic implants |
UNE-EN ISO 11135:2015
|
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) |
AAMI ISO TIR 17665-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ANSI/AAMI/ISO 17665-1 |
I.S. EN ISO 14457:2017
|
DENTISTRY - HANDPIECES AND MOTORS (ISO 14457:2017) |
ANSI/AAMI/IEC 80601-2-58:2014
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
UNE-EN ISO 7494-1:2012
|
Dentistry - Dental units - Part 1: General requirements and test methods (ISO 7494-1:2011) |
I.S. EN 13060:2014
|
SMALL STEAM STERILIZERS |
CSA C22.2 No. 80601-2-60 : 2014
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-60: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF DENTAL EQUIPMENT |
CEI UNI EN 1041 : 2014
|
INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
CSA Z17665-2:09 (R2019)
|
Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009, IDT) |
ISO 9873:2017
|
Dentistry Intra-oral mirrors |
DIN EN ISO 19715:2016-03 (Draft)
|
DENTISTRY - FILLING INSTRUMENT WITH CONTRA ANGLE (ISO 19715:2017) |
CSA Z17510.2 : 2009
|
SLEEP APNOEA BREATHING THERAPY - PART 2: MASKS AND APPLICATION ACCESSORIES |
I.S. EN ISO 9873:2017
|
DENTISTRY - INTRA-ORAL MIRRORS (ISO 9873:2017) |
UNE-EN ISO 14457:2013
|
Dentistry - Handpieces and motors (ISO 14457:2012) |
NF EN ISO 11953 : 2010
|
DENTISTRY - IMPLANTS - CLINICAL PERFORMANCE OF HAND TORQUE INSTRUMENTS |
I.S. EN ISO 16635-2:2014
|
DENTISTRY - DENTAL RUBBER DAM INSTRUMENTS - PART 2: CLAMP FORCEPS (ISO 16635-2:2014) |
UNI EN ISO 11135 : 2014
|
STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
EN ISO 14937:2009
|
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009) |
DIN EN 1639:2010-02
|
Dentistry - Medical devices for dentistry - Instruments |
DIN EN ISO 6875:2011-10
|
DENTISTRY - PATIENT CHAIR |
DIN EN 556-2:2015-11
|
STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 2: REQUIREMENTS FOR ASEPTICALLY PROCESSED MEDICAL DEVICES |
DIN EN 1041:2013-12
|
Information supplied by the manufacturer of medical devices (includes Amendment A1:2013) |
DIN EN ISO 17665-1:2006-11
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
DIN EN ISO 17510-2:2009-07
|
SLEEP APNOEA BREATHING THERAPY - PART 2: MASKS AND APPLICATION ACCESSORIES |
DIN EN 1640:2010-02
|
Dentistry - Medical devices for dentistry - Equipment |
DIN EN ISO 17510-1:2009-07
|
Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy equipment (ISO 17510-1:2007) |
BS EN 556-2:2015
|
Sterilization of medical devices. Requirements for medical devices to be designated \'STERILE\' Requirements for aseptically processed medical devices |
BS EN ISO 15883-2:2009
|
Washer-disinfectors Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc. |
BS EN 1640:2009
|
Dentistry. Medical devices for dentistry. Equipment |
BS EN 1639:2009
|
Dentistry. Medical devices for dentistry. Instruments |
BS EN ISO 22442-1:2015
|
Medical devices utilizing animal tissues and their derivatives Application of risk management |
ISO 25424:2009
|
Sterilization of medical devices Low temperature steam and formaldehyde Requirements for development, validation and routine control of a sterilization process for medical devices |
I.S. EN ISO 6875:2011
|
DENTISTRY - PATIENT CHAIR |
I.S. EN ISO 7153-1:2016
|
SURGICAL INSTRUMENTS - MATERIALS - PART 1: METALS (ISO 7153-1:2016) |
I.S. EN ISO 15883-2:2009
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANAESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
I.S. EN ISO 17510-1:2009
|
SLEEP APNOEA BREATHING THERAPY - PART 1: SLEEP APNOEA BREATHING THERAPY EQUIPMENT |
I.S. EN ISO 14937:2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
EN ISO 17510-1:2009
|
Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy equipment (ISO 17510-1:2007) |
I.S. EN ISO 17510-2:2009
|
SLEEP APNOEA BREATHING THERAPY - PART 2: MASKS AND APPLICATION ACCESSORIES |
I.S. EN ISO 22442-1:2015
|
MEDICAL DEVICES UTILIZING ANIMAL TISSUES AND THEIR DERIVATIVES - PART 1: APPLICATION OF RISK MANAGEMENT (ISO 22442-1:2015) |
I.S. EN 1639:2009
|
DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
I.S. EN 1640:2009
|
DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - EQUIPMENT |
EN ISO 22442-1:2015
|
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) |
I.S. EN ISO 9173-1:2016
|
DENTISTRY - EXTRACTION FORCEPS - PART 1: GENERAL REQUIREMENTS (ISO 9173-1:2016) |
I.S. EN ISO 10451:2010
|
DENTISTRY - CONTENTS OF TECHNICAL FILE FOR DENTAL IMPLANT SYSTEMS |
I.S. EN ISO 14630:2012
|
NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 14630:2012) |
VDI 2083 Blatt 13.2:2009-01
|
Cleanroom technology - Quality, production and distribution of ultrapure water - Microelectronics and other technical applications |
VDI 2083 Blatt 13.1:2009-01
|
Cleanroom technology - Quality, production and distribution of ultrapure water - Fundamentals |
DIN EN ISO 16635-2 E : 2014
|
DENTISTRY - DENTAL RUBBER DAM INSTRUMENTS - PART 2: CLAMP FORCEPS (ISO 16635-2:2014) |
04/30048118 DC : DRAFT MAY 2004
|
BS EN ISO 11135 - STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
14/30278521 DC : 0
|
BS EN ISO 18556 - DENTISTRY - INTRAORAL SPATULAS |
13/30242570 DC : 0
|
BS ISO 8828 - IMPLANTS FOR SURGERY - GUIDANCE ON CARE AND HANDLING OF ORTHOPAEDIC IMPLANTS |
13/30285624 DC : 0
|
BS EN ISO 16061 - INSTRUMENTATION FOR USE IN ASSOCIATION WITH NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
PD IEC/TR 60601-4-1:2017
|
Medical electrical equipment Guidance and interpretation. Medical electrical equipment and medical electrical systems employing a degree of autonomy |
11/30215841 DC : 0
|
BS EN ISO 14457 - DENTISTRY - HAND PIECES AND MOTORS |
DIN EN ISO 18556 E : 2016
|
DENTISTRY - INTRAORAL SPATULAS (ISO 18556:2016) |
I.S. EN ISO 17665-1:2006
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
DIN EN ISO 80601-2-72 E : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS (ISO 80601-2-72:2015) |
DIN EN ISO 18397 E : 2016
|
DENTISTRY - POWERED SCALER (ISO 18397:2016) |
14/30290166 DC : 0
|
BS ISO 16142-1 - MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 1: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL NON-IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
AAMI ISO 10651-5 : 2006
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
BS EN ISO 3630-4:2009
|
Dentistry. Root canal instruments Auxiliary instruments |
DIN EN ISO 18556:2016-09
|
DENTISTRY - INTRAORAL SPATULAS (ISO 18556:2016) |
NF EN ISO 80601-2-56 : 2017
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-56: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CLINICAL THERMOMETERS FOR BODY TEMPERATURE MEASUREMENT |
UNI EN ISO 80601-2-69 : 2014
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-69: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF OXYGEN CONCENTRATOR EQUIPMENT |
BS EN ISO 80601-2-69:2014
|
Medical electrical equipment Particular requirements for basic safety and essential performance of oxygen concentrator equipment |
09/30193875 DC : DRAFT JAN 2009
|
BS EN ISO 11953 - DENTISTRY - THE PERFORMANCE OF HAND TORQUE INSTRUMENTS FOR THE CLINICAL TIGHTENING OF SCREW-RETAINED JOINTS IN ENDOSSEOUS DENTAL IMPLANT SYSTEMS |
EN 1041:2008+A1:2013
|
Information supplied by the manufacturer of medical devices |
UNI EN ISO 25424 : 2011
|
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
04/300654 DC : DRAFT JAN 2004
|
BS EN ISO 14630 - NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
BS ISO 16142-1:2016
|
Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
UNE-EN ISO 9168:2010
|
Dentistry - Hose connectors for air driven dental handpieces (ISO 9168:2009) |
BS ISO 10651-5:2006
|
Lung ventilators for medical use. Particular requirements for basic safety and essential performance Gas-powered emergency resuscitators |
17/30338806 DC : 0
|
BS EN ISO 25424 - STERILIZATION OF HEALTH CARE PRODUCTS - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNI EN ISO 11953 : 2010
|
DENTISTRY - IMPLANTS - CLINICAL PERFORMANCE OF HAND TORQUE INSTRUMENTS |
BS EN 15546-1:2008
|
Small bore connectors for liquids and gases in healthcare applications General requirements |
16/30346835 DC : 0
|
BS ISO 20789 - ANAESTHETIC AND RESPIRATORY EQUIPMENT - PASSIVE HUMIDIFIERS |
I.S. EN ISO 19490:2017
|
DENTISTRY - SINUS MEMBRANE ELEVATOR (ISO 19490:2017) |
BS EN ISO 11135:2014
|
Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices |
CSA Z11135-1 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
ANSI/AAMI/ISO 22442-1:2016
|
MEDICAL DEVICES UTILIZING ANIMAL TISSUES AND THEIR DERIVATIVES - PART 1: APPLICATION OF RISK MANAGEMENT |
DIN EN ISO 19490 E : 2017
|
DENTISTRY - SINUS MEMBRANE ELEVATOR (ISO 19490:2017) |
ISO 18397:2016
|
Dentistry Powered scaler |
AAMI ST15883-2 : 2013
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
CSA Z17665-1:09 (R2019)
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 17665-1:2006, first edition, 2006-08-15, with Canadian deviations) |
DIN EN ISO 19490:2016-07 (Draft)
|
DENTISTRY - SINUS MEMBRANE ELEVATOR (ISO 19490:2017) |
I.S. EN ISO 20608:2018
|
DENTISTRY - POWDER JET HANDPIECES AND POWDERS (ISO 20608:2018) |
EN 13060:2014
|
Small steam sterilizers |
ANSI/AAMI ISO 17665-1:2006(R2013)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
AAMI ISO 14937:2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNI CEN ISO/TS 11135-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
CSA Z17665-1 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
I.S. EN ISO 25424:2011
|
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
IEC TR 60601-4-1:2017
|
Medical electrical equipment - Part 4-1: Guidance and interpretation - Medical electrical equipment and medical electrical systems employing a degree of autonomy |
AAMI ISO 11135-1 : 2007
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
BS EN 80601-2-58:2015
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
OVE/ONORM EN ISO 80601-2-55 : 2012
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS (ISO 80601-2-55:2011) |
I.S. EN ISO 13504:2012
|
DENTISTRY - GENERAL REQUIREMENTS FOR INSTRUMENTS AND RELATED ACCESSORIES USED IN DENTAL IMPLANT PLACEMENT AND TREATMENT (ISO 13504:2012) |
EN ISO 80601-2-55:2018
|
Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors (ISO 80601-2-55:2018) |
I.S. EN ISO 7492:2018
|
DENTISTRY - DENTAL EXPLORER (ISO 7492:2018) |
ISO 22374:2005
|
Dentistry Dental handpieces Electrical-powered scalers and scaler tips |
ISO 7492:2018
|
Dentistry — Dental explorer |
DIN EN 13060:2015-03
|
SMALL STEAM STERILIZERS |
ISO 80601-2-69:2014
|
Medical electrical equipment Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment |
ISO 9173-1:2016
|
Dentistry — Extraction forceps — Part 1: General requirements |
EN ISO 80601-2-69:2014
|
Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014) |
EN ISO 9173-1:2016
|
Dentistry - Extraction forceps - Part 1: General requirements (ISO 9173-1:2016) |
EN ISO 17937:2015
|
Dentistry - Osteotome (ISO 17937:2015) |
UNI EN ISO 6875 : 2011
|
DENTISTRY - PATIENT CHAIR |
UNI EN 1640 : 2010
|
DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - EQUIPMENT |
UNI EN ISO 10451 : 2010
|
DENTISTRY - CONTENTS OF TECHNICAL FILE FOR DENTAL IMPLANT SYSTEMS |
UNI EN 1639 : 2010
|
DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
UNI EN ISO 17510-2 : 2009
|
SLEEP APNOEA BREATHING THERAPY - PART 2: MASKS AND APPLICATION ACCESSORIES |
UNI EN ISO 15883-2 : 2009
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER- DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANAESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
UNI EN ISO 14937 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
EN 15546-1:2008
|
Small bore connectors for liquids and gases in healthcare applications - Part 1 - General Requirements |
UNI EN ISO 14630 : 2013
|
NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
UNI CEI EN 15546-1 : 2009
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
UNI EN ISO 9168 : 2009
|
DENTISTRY - HOSE CONNECTORS FOR AIR DRIVEN DENTAL HANDPIECES |
DIN EN ISO 19715 E : 2017
|
DENTISTRY - FILLING INSTRUMENT WITH CONTRA ANGLE (ISO 19715:2017) |
DIN EN ISO 25424:2011-09
|
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
DIN EN ISO 13504:2012-10
|
DENTISTRY - GENERAL REQUIREMENTS FOR INSTRUMENTS AND RELATED ACCESSORIES USED IN DENTAL IMPLANT PLACEMENT AND TREATMENT (ISO 13504:2012) |
DIN EN ISO 20857 E : 2013
|
STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 20857:2010) |
16/30302544 DC : 0
|
BS EN ISO 9873 - DENTISTRY - INTRA-ORAL MIRRORS |
18/30372409 DC : DRAFT APR 2018
|
BS EN ISO 3630-1 - DENTISTRY - ENDODONTIC INSTRUMENTS - PART 1: GENERAL REQUIREMENTS |
DIN EN ISO 9873:2016-03 (Draft)
|
DENTISTRY - INTRA-ORAL MIRRORS (ISO 9873:2017) |
I.S. EN 556-2:2015
|
STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 2: REQUIREMENTS FOR ASEPTICALLY PROCESSED MEDICAL DEVICES |
BS EN ISO 9168:2009
|
Dentistry. Hose connectors for air driven dental handpieces |
13/30264413 DC : 0
|
BS EN ISO 80601-2-72 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS |
BS EN ISO 18397:2016
|
Dentistry. Powered scaler |
BS EN ISO 11953:2010
|
Dentistry. Implants. Clinical performance of hand torque instruments |
I.S. EN ISO 11135-1:2007
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
UNE-EN ISO 20857:2013
|
Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) |
BS EN 80601-2-60:2015
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of dental equipment |
CSA Z17665-2:09 (R2019)
|
Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (Adopted ISO/TS 17665-2:2009, first edition, 2009-01-15) |
08/30168843 DC : DRAFT MAR 2008
|
BS EN ISO 9168 - DENTISTRY - HOSE CONNECTORS FOR AIR DRIVEN DENTAL HANDPIECES |
UNE-EN ISO 3630-4:2010
|
Dentistry - Root canal instruments - Part 4: Auxiliary instruments (ISO 3630-4:2009) |
CAN/CSA-C22.2 NO. 80601-2-70:17
|
Medical electrical equipment — Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment (Adopted ISO 80601-2-70:2015, first edition, 2015-01 , with Canadian deviations) |
UNI EN ISO 13504 : 2012
|
DENTISTRY - GENERAL REQUIREMENTS FOR INSTRUMENTS AND RELATED ACCESSORIES USED IN DENTAL IMPLANT PLACEMENT AND TREATMENT |
UNI CEI EN 1041 : 2013
|
INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
04/30081258 DC : DRAFT MARCH 2004
|
BS EN ISO 11737-1 - STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 1 - DETERMINATION OF A POPULATION OF MICRO ORGANISMS ON PRODUCTS |
17/30323194 DC : 0
|
BS EN ISO 20569 - DENTISTRY - TREPHINE BURS |
08/30168812 DC : DRAFT FEB 2008
|
BS ISO 3630-4 - DENTISTRY - ROOT CANAL INSTRUMENTS - PART 4: AUXILIARY INSTRUMENTS |
17/30323197 DC : 0
|
BS EN ISO 20570 - DENTISTRY - ORAL SURGICAL SCALPEL HANDLE |
BS ISO 20308:2017
|
Traditional Chinese medicine. Gua Sha instruments |
DIN EN ISO 17937 E : 2016
|
DENTISTRY - OSTEOTOME (ISO 17937:2015) |
BS EN ISO 9873:2017
|
Dentistry. Intra-oral mirrors |
UNI EN ISO 21672-1 : 2012
|
DENTISTRY - PERIODONTAL PROBES - PART 1: GENERAL REQUIREMENTS |
NF EN ISO 80601-2-12 : 2011
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
BS EN ISO 22374:2005
|
Dentistry. Dental handpieces. Electrical-powered scalers and scaler tips |
CSA Z11135-1 :2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
CSA Z11135-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
UNI EN ISO 20857 : 2013
|
STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
CSA Z11135-1 : 2009 : FR
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
DIN EN ISO 20857:2013-08
|
Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) |
ISO 80601-2-56:2017
|
Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement |
I.S. EN ISO 11135:2014
|
STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11135:2014) |
I.S. EN ISO 7494-1:2011
|
DENTISTRY - DENTAL UNITS - PART 1: GENERAL REQUIREMENTS AND TEST METHODS |
BS EN ISO 7492:2018
|
Dentistry. Dental explorer |
AAMI/ISO TIR17665-2:2009(R2016)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ANSI/AAMI/ISO 17665-1 |
I.S. EN ISO 80601-2-72:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS (ISO 80601-2-72:2015) |
S.R. CEN ISO TS 11135-2:2008
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
DIN EN ISO 9873 E : 2000
|
DENTISTRY - INTRA-ORAL MIRRORS (ISO 9873:2017) |
UNI EN ISO 17510-1 : 2009
|
SLEEP APNOEA BREATHING THERAPY - PART 1: SLEEP APNOEA BREATHING THERAPY EQUIPMENT |
ISO 17510:2015
|
Medical devices — Sleep apnoea breathing therapy — Masks and application accessories |
BS EN ISO 7494-1:2011
|
Dentistry. Dental units General requirements and test methods |
UNI EN ISO 80601-2-55 : 2012
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
UNE-EN 13060:2015
|
Small steam sterilizers |
EN ISO 9873:2017
|
Dentistry - Intra-oral mirrors (ISO 9873:2017) |
ISO 80601-2-55:2018
|
Medical electrical equipment — Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors |
EN ISO 20608:2018
|
Dentistry - Powder jet handpieces and powders (ISO 20608:2018) |
ISO 80601-2-70:2015
|
Medical electrical equipment Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment |
I.S. EN ISO 80601-2-12:2011
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS (ISO 80601-2-12:2011/COR 1:2011) |
I.S. EN ISO 16061:2015
|
INSTRUMENTATION FOR USE IN ASSOCIATION WITH NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 16061:2015) |
ISO 10651-5:2006
|
Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 5: Gas-powered emergency resuscitators |
EN ISO 80601-2-12:2011/AC:2011
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS (ISO 80601-2-12:2011/COR 1:2011) |
ISO 80601-2-12:2011
|
Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators |
UNE-EN ISO 6875:2012
|
Dentistry - Patient chair (ISO 6875:2011) |
DIN EN ISO 14630:2013-03
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
ISO 14937:2009
|
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 13504:2012
|
Dentistry — General requirements for instruments and related accessories used in dental implant placement and treatment |
ISO 19715:2017
|
Dentistry — Filling instrument with contra angle |
BS EN ISO 17510-1:2009
|
Sleep apnoea breathing therapy Sleep apnoea breathing therapy equipment |
UNE-EN 556-2:2016
|
Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE" - Part 2: Requirements for aseptically processed medical devices |
ISO 3630-4:2009
|
Dentistry — Root canal instruments — Part 4: Auxiliary instruments |
ISO 17937:2015
|
Dentistry Osteotome |
ISO 20857:2010
|
Sterilization of health care products Dry heat Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 16061:2015
|
Instrumentation for use in association with non-active surgical implants General requirements |
ISO 17510-2:2007
|
Sleep apnoea breathing therapy Part 2: Masks and application accessories |
ISO 7153-1:2016
|
Surgical instruments Materials Part 1: Metals |
ISO 21672-1:2012
|
Dentistry — Periodontal probes — Part 1: General requirements |
IEC 80601-2-60:2012
|
Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment |
UNE-EN ISO 7153-1:2017
|
Surgical instruments - Materials - Part 1: Metals (ISO 7153-1:2016) |
IEC 80601-2-58:2014+AMD1:2016 CSV
|
Medical electrical equipment - Part 2-58: Particular requirementsfor the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
BS EN ISO 17665-1:2006
|
Sterilization of health care products. Moist heat Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 22442-1:2015
|
Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management |
BS EN ISO 14937:2009
|
Sterilization of health care products. General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 80601-2-72:2015
|
Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients |
ANSI/AAMI ST15883-2:2013(R2015) (ISO 15883-2:2006 MOD)
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
UNE-EN 1041:2009
|
Information supplied by the manufacturer of medical devices |
ISO 16635-2:2014
|
Dentistry Dental rubber dam instruments Part 2: Clamp forceps |
EN 80601-2-60:2015
|
Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment |
ISO 17665-1:2006
|
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
BS EN 13060 : 2014
|
SMALL STEAM STERILIZERS |
ISO 6875:2011
|
Dentistry Patient chair |
ISO 18556:2016
|
Dentistry Intraoral spatulas |
ISO 11953:2010
|
Dentistry Implants Clinical performance of hand torque instruments |
ISO/TS 11135-2:2008
|
Sterilization of health care products Ethylene oxide Part 2: Guidance on the application of ISO 11135-1 |
BS EN ISO 9173-1:2016
|
Dentistry. Extraction forceps General requirements |
BS EN 1041 : 2008
|
INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
ISO 9168:2009
|
Dentistry Hose connectors for air driven dental handpieces |
BS EN ISO 6875:2011
|
Dentistry. Patient chair |
UNE-EN ISO 14937:2010
|
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009) |
UNE-EN ISO 14630:2013
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
BS EN ISO 10451:2010
|
Dentistry. Contents of technical file for dental implant systems |
ISO 19490:2017
|
Dentistry — Sinus membrane elevator |
ISO 10451:2010
|
Dentistry — Contents of technical file for dental implant systems |
UNE-EN ISO 9873:2017
|
Dentistry - Intra-oral mirrors (ISO 9873:2017) |
EN 15424:2007
|
Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices |
EN ISO 80601-2-72:2015
|
Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (ISO 80601-2-72:2015) |
EN ISO 11135-1:2007
|
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007) |
EN ISO 18556:2016
|
Dentistry - Intraoral spatulas (ISO 18556:2016) |
EN ISO 11953:2010
|
Dentistry - Implants - Clinical performance of hand torque instruments (ISO 11953:2010) |
EN ISO 7153-1:2016
|
Surgical instruments - Materials - Part 1: Metals (ISO 7153-1:2016) |
EN ISO 9168:2009
|
Dentistry - Hose connectors for air driven dental handpieces (ISO 9168:2009) |
EN ISO 15883-2:2009
|
Washer-disinfectors - Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc. (ISO 15883-2:2006) |
EN ISO 19490:2017
|
Dentistry - Sinus membrane elevator (ISO 19490:2017) |
EN ISO 17510-2:2009
|
Sleep apnoea breathing therapy - Part 2: Masks and application accessories (ISO 17510-2:2007) |
EN ISO 25424:2011
|
Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) |
EN 1639:2009
|
Dentistry - Medical devices for dentistry - Instruments |
EN 556-2:2015
|
Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE" - Part 2: Requirements for aseptically processed medical devices |
EN ISO 10451:2010
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Dentistry - Contents of technical file for dental implant systems (ISO 10451:2010) |
EN ISO 20857:2013
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Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) |
EN 1640:2009
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Dentistry - Medical devices for dentistry - Equipment |
EN ISO 16635-2:2014
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Dentistry - Dental rubber dam instruments - Part 2: Clamp forceps(ISO 16635-2:2014) |
EN ISO 19715:2017
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Dentistry - Filling instrument with contra angle (ISO 19715:2017) |
EN ISO 17665-1 : 2006
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Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
EN ISO 21672-1:2012
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Dentistry - Periodontal probes - Part 1: General requirements (ISO 21672-1:2012) |
EN ISO 14630:2012
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Non-active surgical implants - General requirements (ISO 14630:2012) |
EN ISO 18397:2016
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Dentistry - Powered scaler (ISO 18397:2016) |
EN ISO 3630-4:2009
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Dentistry - Root canal instruments - Part 4: Auxiliary instruments (ISO 3630-4:2009) |
EN ISO 13504:2012
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Dentistry - General requirements for instruments and related accessories used in dental implant placement and treatment (ISO 13504:2012) |
EN ISO 6875:2011
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Dentistry - Patient chair (ISO 6875:2011) |
BS ISO 8828:2014
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Implants for surgery. Guidance on care and handling of orthopaedic implants |
BS EN ISO 16061:2015
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Instrumentation for use in association with non-active surgical implants. General requirements |
UNE-EN ISO 21672-1:2012
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Dentistry - Periodontal probes - Part 1: General requirements (ISO 21672-1:2012) |
UNI EN ISO 3630-4 : 2009
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DENTISTRY - ROOT CANAL INSTRUMENTS - PART 4: AUXILIARY INSTRUMENTS |
BS EN ISO 25424:2011
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Sterilization of medical devices. Low temperature steam and formaldehyde. Requirements for development, validation and routine control of a sterilization process for medical devices |
13/30290370 DC : 0
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BS ISO 17510 - MEDICAL DEVICES - SLEEP APNOEA BREATHING THERAPY - MASKS AND APPLICATION ACCESSORIES |
BS ISO 27427:2013
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Anaesthetic and respiratory equipment. Nebulizing systems and components |
14/30273278 DC : 0
|
BS EN ISO 18397 - DENTISTRY - POWERED SCALER |
UNE-EN ISO 17937:2016
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Dentistry - Osteotome (ISO 17937:2015) |
17/30303088 DC : 0
|
BS EN ISO 7492 - DENTISTRY - DENTAL EXPLORER |
BS EN ISO 18556:2016
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Dentistry. Intraoral spatulas |
15/30300279 DC : 0
|
BS ISO 80601-2-74 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-74: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY HUMIDIFYING EQUIPMENT |
17/30326683 DC : DRAFT SEP 2017
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BS ISO 19979 - OPHTHALMIC OPTICS - CONTACT LENSES - HYGIENIC MANAGEMENT OF MULTIPATIENT USE TRIAL CONTACT LENSES |
13/30271473 DC : 0
|
BS EN 80601-2-58 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
DD CEN ISO/TS 17665-2:2009
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Sterilization of health care products. Moist heat Guidance on the application of ISO 17665-1 |
16/30310949 DC : 0
|
BS ISO 5910 - CARDIOVASCULAR IMPLANTS AND EXTRACOPOREAL SYSTEMS - CARDIAC VALVE REPAIR DEVICES |
17/30332162 DC : 0
|
BS EN ISO 7494-1 - DENTISTRY - STATIONARY DENTAL UNITS AND DENTAL PATIENT CHAIRS - PART 1: GENERAL REQUIREMENTS AND TEST METHODS |
S.R. CEN ISO/TS 17665-2:2009
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STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
07/30164697 DC : 0
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ISO 20857 - STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF AN INDUSTRIAL STERILIZATION PROCESS FOR MEDICAL DEVICES |
BS EN ISO 17937:2015
|
Dentistry. Osteotome |
CSA Z11135 : 2015
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STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
CSA Z11135-2 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ISO 11135-1 |
AAMI ISO 20857 : 2010
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STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
ISO 19611:2017
|
Traditional Chinese medicine — Air extraction cupping device |
CSA ISO 14937 : 2011 : R2016
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STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
CSA Z17510.1 : 2010
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SLEEP APNOEA BREATHING THERAPY - PART 1: SLEEP APNOEA BREATHING THERAPY EQUIPMENT |
EN ISO 11135:2014
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Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) |
CSA Z15883-2 : 2009 : R2014
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANAESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
CSA Z10651-5 : 2008 : R2018
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Lung Ventilators for Medical Use - Particular Requirements for Basic Safety and Essential Performance - Part 5: Gas-Powered Emergency Resuscitators |
DIN EN ISO 80601-2-69:2014-12
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Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014) |
I.S. EN ISO 19715:2017
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DENTISTRY - FILLING INSTRUMENT WITH CONTRA ANGLE (ISO 19715:2017) |
CSA C22.2 No. 80601-2-58 : 2010
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
AAMI ISO TIR 17665-3:2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - GUIDANCE ON THE DESIGNATION OF A MEDICAL PRODUCT TO A PRODUCT FAMILY AND PROCESSING CATEGORY FOR STEAM STERILIZATION |
I.S. EN ISO 9168:2009
|
DENTISTRY - HOSE CONNECTORS FOR AIR DRIVEN DENTAL HANDPIECES |
I.S. EN ISO 3630-4:2009
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DENTISTRY - ROOT CANAL INSTRUMENTS - PART 4: AUXILIARY INSTRUMENTS |
I.S. EN ISO 80601-2-55:2018
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS (ISO 80601-2-55:2018) |
ISO 80601-2-67:2014
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Medical electrical equipment Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment |
I.S. EN ISO 20857:2013
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STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 20857:2010) |
ISO/TR 14283:2018
|
Implants for surgery Essential principles of safety and performance |
I.S. EN ISO 80601-2-69:2014
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-69: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF OXYGEN CONCENTRATOR EQUIPMENT (ISO 80601-2-69:2014) |
CSA Z15883-2 : 2009
|
WASHER-DISINFECTORS - PART 2: REQUIREMENTS AND TESTS FOR WASHER-DISINFECTORS EMPLOYING THERMAL DISINFECTION FOR SURGICAL INSTRUMENTS, ANAESTHETIC EQUIPMENT, BOWLS, DISHES, RECEIVERS, UTENSILS, GLASSWARE, ETC. |
ISO/TS 17665-3:2013
|
Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization |
EN ISO 7492:2018
|
Dentistry - Dental explorer (ISO 7492:2018) |
EN ISO 22374:2005
|
Dentistry - Dental handpieces - Electrical-powered scalers and scaler tips (ISO 22374:2005) |
ISO 7494-1:2011
|
Dentistry Dental units Part 1: General requirements and test methods |
BS ISO 19979:2018
|
Ophthalmic optics. Contact lenses. Hygienic management of multipatient use trial contact lenses |
EN ISO 7494-1:2011
|
Dentistry - Dental units - Part 1: General requirements and test methods (ISO 7494-1:2011) |
17/30362728 DC : 0
|
BS EN 17169 - TATTOOING - SAFE AND HYGIENIC PRACTICE |
ISO 20608:2018
|
Dentistry — Powder jet handpieces and powders |
13/30254355 DC : 0
|
BS ISO 80601-2-70 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-70: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF SLEEP APNEOA BREATHING THERAPY EQUIPMENT |
AAMI ISO TIR 11135-2 : 2008
|
STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 2: GUIDANCE ON THE APPLICATION OF ANSI/AAMI/ISO 11135-1 |
DIN EN ISO 7494-1:2011-11
|
DENTISTRY - DENTAL UNITS - PART 1: GENERAL REQUIREMENTS AND TEST METHODS (ISO 7494-1:2011) |
UNE-EN ISO 25424:2011
|
Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) |
EN ISO 14457:2017
|
Dentistry - Handpieces and motors (ISO 14457:2017) |
EN ISO 80601-2-56:2017
|
Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement (ISO 80601-2-56:2017) |
I.S. EN ISO 22374:2005
|
DENTISTRY - DENTAL HANDPIECES - ELECTRICAL-POWERED SCALERS AND SCALER TIPS |
ISO 11135:2014
|
Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices |
I.S. EN 80601-2-58:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
ISO 27427:2013
|
Anaesthetic and respiratory equipment — Nebulizing systems and components |
ISO 14457:2017
|
Dentistry — Handpieces and motors |
DIN EN ISO 10451:2010-11
|
Dentistry - Contents of technical file for dental implant systems (ISO 10451:2010) |
DIN EN ISO 9173-1 E : 2017
|
DENTISTRY - EXTRACTION FORCEPS - PART 1: GENERAL REQUIREMENTS (ISO 9173-1:2016) |
DIN EN ISO 9173-1:2015-02 (Draft)
|
DENTISTRY - EXTRACTION FORCEPS - PART 1: GENERAL REQUIREMENTS (ISO 9173-1:2016) |
BS EN ISO 17510-2:2009
|
Sleep apnoea breathing therapy Masks and application accessories |
BS EN ISO 11135-1:2007
|
Sterilization of health care products. Ethylene oxide Requirements for development, validation and routine control of a sterilization process for medical devices |
ISO 17510-1:2007
|
Sleep apnoea breathing therapy Part 1: Sleep apnoea breathing therapy equipment |
ISO 14630:2012
|
Non-active surgical implants General requirements |
ISO/TS 17665-2:2009
|
Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1 |
EN ISO 16061:2015
|
Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
DIN EN ISO 9173-1:2017-03
|
DENTISTRY - EXTRACTION FORCEPS - PART 1: GENERAL REQUIREMENTS (ISO 9173-1:2016) |
DIN EN ISO 9873:2000-07
|
DENTISTRY - INTRA-ORAL MIRRORS (ISO 9873:2017) |
DIN EN ISO 14937:2010-03
|
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009) |
EN 15546-1 : 2008
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
CEN ISO/TS 17665-2:2009
|
Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009) |