03/108542 DC : DRAFT MAY 2003
|
BS EN ISO 11140-1 - STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS |
I.S. EN ISO 5840:2009
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
BS EN ISO 23328-2:2009
|
Breathing system filters for anaesthetic and respiratory use Non-filtration aspects |
04/300654 DC : DRAFT JAN 2004
|
BS EN ISO 14630 - NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
CSA ISO 11712 : 2014
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - SUPRALARYNGEAL AIRWAYS AND CONNECTORS |
CSA Z10651-5 : 2008 : R2013
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
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 |
CSA Z9360.2:2007
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 2: HMES FOR USE WITH TRACHEOSTOMIZED PATIENTS HAVING MINIMUM TIDAL VOLUMES OF 250 ML |
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 |
CSA Z11140.1 : 2007 : R2012
|
STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS |
DIN EN ISO 8836:2015-02
|
Suction catheters for use in the respiratory tract (ISO 8836:2014); German version EN ISO 8836:2014 |
ASTM F 2761 : 2009 : R2013
|
Medical Devices and Medical Systems - Essential safety requirements for equipment comprising the patient-centric integrated clinical environment (ICE) - Part 1: General requirements and conceptual model |
BS EN ISO 22803:2005
|
Dentistry. Membrane materials for guided tissue regeneration in oral and maxillofacial surgery. Contents of a technical file |
DIN EN ISO 23328-2:2009-07
|
BREATHING SYSTEM FILTERS FOR ANAESTHETIC AND RESPIRATORY USE - PART 2: NON-FILTRATION ASPECTS |
EN ISO 23328-2:2009
|
Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (ISO 23328-2:2002) |
EN 1282-2:2005+A1:2009
|
Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified) |
CEN ISO/TR 14969:2005
|
Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004) |
EN ISO 5366-1:2009
|
Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000) |
EN 13503-6 : 2002
|
OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 6: SHELF-LIFE AND TRANSPORT STABILITY |
BS ISO 10651-5:2006
|
Lung ventilators for medical use. Particular requirements for basic safety and essential performance Gas-powered emergency resuscitators |
14/30281560 DC : 0
|
BS EN ISO 5840-2 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES |
04/30109833 DC : 0
|
ISO 8836 - SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
07/30169940 DC : 0
|
BS EN ISO 11979-4 - OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 4: LABELLING AND INFORMATION |
03/103026 DC : DRAFT JAN 2003
|
BS EN ISO 5840 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
AAMI ISO 5840 : 2005 : R2010
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
CSA Z9360.1 : 2007
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 1: HMES FOR USE WITH MINIMUM TIDAL VOLUMES OF 250 ML |
CSA Z9360.2 : 2007:R2012
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 2: HMES FOR USE WITH TRACHEOSTOMIZED PATIENTS HAVING MINIMUM TIDAL VOLUMES OF 250 ML |
AAMI ISO 5840 :2005
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
CSA Z10651-5 : 2008
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
BIS IS/ISO 14708-1 : 2000
|
IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER |
UNI EN ISO 23328-2 : 2009
|
BREATHING SYSTEM FILTERS FOR ANAESTHETIC AND RESPIRATORY USE - PART 2: NON-FILTRATION ASPECTS |
ISO/TS 15539:2000
|
Cardiovascular implants Endovascular prostheses |
CSA ISO 11712:14 (R2019)
|
Anaesthetic and respiratory equipment - Supralaryngeal airways and connectors (Adopted ISO 11712:2009, first edition, 2009-05-15) |
DIN EN ISO 22610:2015-12 (Draft)
|
SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES, FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - TEST METHOD TO DETERMINE THE RESISTANCE TO WET BACTERIAL PENETRATION |
DIN EN ISO 22803:2006-01
|
Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
BS EN ISO 9360-1:2009
|
Anaesthetic and respiratory equipment. Heat and moisture exchangers (HMEs) for humidifying respired gases in humans HMEs for use with minimal tidal volumes of 250 ml |
I.S. EN ISO 5366-1:2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES - PART 1: TUBES AND CONNECTORS FOR USE IN ADULTS |
DIN EN 1820:2009-12
|
ANAESTHETIC RESERVOIR BAGS |
I.S. EN ISO 9360-1:2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 1: HMES FOR USE WITH MINIMUM TIDAL VOLUMES OF 250 ML |
I.S. EN ISO 9360-2:2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 2: HMES FOR USE WITH TRACHEOSTOMIZED PATIENTS HAVING MINIMUM TIDAL VOLUMES OF 250 ML |
DIN EN 13503-6:2003-03
|
OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 6: SHELF-LIFE AND TRANSPORT STABILITY |
I.S. EN 1282-2:2005
|
TRACHEOSTOMY TUBES - PART 2: PAEDIATRIC TUBES |
DIN EN ISO 5366-1:2009-07
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES - PART 1: TUBES AND CONNECTORS FOR USE IN ADULTS |
05/30138123 DC : DRAFT AUG 2005
|
BS ISO 8836 - SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
05/30097406 DC : DRAFT JUL 2005
|
ISO 11979-6 - OPHTHALMIC INSTRUMENTS - INTRAOCULAR LENSES - PART 6: SHELF-LIFE AND TRANSPORT STABILITY |
AAMI ISO 10651-5 : 2006
|
LUNG VENTILATORS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - PART 5: GAS-POWERED EMERGENCY RESUSCITATORS |
I.S. CEN ISO TR 14969:2005
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485: 2003 |
BS PD ISO/TR 14969 : 2004 AMD 15958
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
AAMI ISO TIR 14969 : 2004
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
15/30329923 DC : 0
|
BS EN ISO 22610 - SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES, FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - TEST METHOD TO DETERMINE THE RESISTANCE TO WET BACTERIAL PENETRATION |
BS ISO 25539-1 : 2003
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES |
03/101659 DC : DRAFT JAN 2003
|
ISO 22803 - DENTISTRY - MEMBRANE MATERIALS FOR GUIDED TISSUE REGENERATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
ISO 11712:2009
|
Anaesthetic and respiratory equipment — Supralaryngeal airways and connectors |
UNI EN ISO 17664 : 2005
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
I.S. EN ISO 23328-2:2009
|
BREATHING SYSTEM FILTERS FOR ANAESTHETIC AND RESPIRATORY USE - PART 2: NON-FILTRATION ASPECTS |
ISO 9360-2:2001
|
Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml |
BS EN ISO 22610:2006
|
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment. Test method to determine the resistance to wet bacterial penetration |
ISO 5840:2005
|
Cardiovascular implants Cardiac valve prostheses |
ISO 22794:2007
|
Dentistry Implantable materials for bone filling and augmentation in oral and maxillofacial surgery Contents of a technical file |
DIN EN ISO 22610:2006-10
|
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006) |
UNE-EN 1282-2:2006
|
Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified) |
I.S. EN 1820:2005
|
ANAESTHETIC RESERVOIR BAGS |
EN ISO 9360-2:2009
|
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001) |
EN ISO 22610:2006
|
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006) |
UNI EN ISO 5840 : 2009
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
UNI EN ISO 5366-1 : 2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES - PART 1: TUBES AND CONNECTORS FOR USE IN ADULTS |
UNI EN ISO 9360-1 : 2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 1: HMES FOR USE WITH MINIMUM TIDAL VOLUMES OF 250 ML |
UNI EN 1282-2 : 2009
|
TRACHEOSTOMY TUBES - PART 2: PAEDIATRIC TUBES |
UNI EN ISO 9360-2 : 2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 2: HMES FOR USE WITH TRACHEOSTOMIZED PATIENTS HAVING MINIMUM TIDAL VOLUMES OF 250 ML |
UNI EN 1820 : 2009
|
ANAESTHETIC RESERVOIR BAGS |
CSA Z17664 : 2006 : R2011
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
ASTM F 2726 : 2008
|
Standard specification for fixation devices for tracheal tubes and other airway devices |
BS ISO 11712:2009
|
Anaesthetic and respiratory equipment. Supralaryngeal airways and connectors |
01/563350 DC : DRAFT AUG 2001
|
BS ISO 25539-1 - CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES |
ISO 13683:1997
|
Sterilization of health care products Requirements for validation and routine control of moist heat sterilization in health care facilities |
11/30219211 DC : 0
|
BS EN ISO 5840-3 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY MINIMALLY INVASIVE TECHNIQUES |
03/314215 DC : DRAFT OCT 2003
|
ISO TR 14969 - MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
12/30244415 DC : DRAFT APR 2012
|
BS ISO 27427 - ANAESTHETIC AND RESPIRATORY EQUIPMENT - NEBULIZING SYSTEMS AND COMPONENTS |
ASTM F 2560 : 2006
|
Standard Specification for Supralaryngeal Airways and Connectors |
CSA ISO TR 14969 : 2005 : R2015
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
AAMI ST81 :2004
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
CSA Z10651-5 : 2008 : R2018
|
Lung Ventilators for Medical Use - Particular Requirements for Basic Safety and Essential Performance - Part 5: Gas-Powered Emergency Resuscitators |
AAMI ST81 : 2004 : R2010
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
ISO/TR 14969:2004
|
Medical devices Quality management systems Guidance on the application of ISO 13485: 2003 |
CSA Z11140.1 : 2007 : R2012 : FR
|
STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS |
CAN/CSA-Z9360-2-07 (R2017)
|
Anaesthetic and Respiratory Equipment - Heat and Moisture Exchangers (HMEs) for Humidifying Respired Gases in Humans - Part 2: HMEs for Use with Tracheostomized Patients Having Minimum Tidal Volumes of 250 ml (Adopted ISO 9360-2:2001, first edition, 2001-04-15, with Canadian deviations) |
CSA Z11140.1 : 2007
|
STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS |
CSA ISO TR 14969 :2005
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
ISO 5366-3:2001
|
Anaesthetic and respiratory equipment Tracheostomy tubes Part 3: Paediatric tracheostomy tubes |
ISO 10651-5:2006
|
Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 5: Gas-powered emergency resuscitators |
DIN EN ISO 9360-1 E : 2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 1: HMES FOR USE WITH MINIMUM TIDAL VOLUMES OF 250 ML |
DIN EN ISO 9360-2 E : 2009
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 2: HMES FOR USE WITH TRACHEOSTOMIZED PATIENTS HAVING MINIMUM TIDAL VOLUMES OF 250 ML |
ISO 9360-1:2000
|
Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 1: HMEs for use with minimum tidal volumes of 250 ml |
BS EN 1820:2005
|
Anaesthetic reservoir bags |
ISO 22610:2006
|
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment Test method to determine the resistance to wet bacterial penetration |
ISO 23328-2:2002
|
Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects |
UNE-EN 1820:2006
|
Anaesthetic reservoir bags (ISO 5362:2000, modified) |
BS EN 1282-2 : 2005
|
TRACHEOSTOMY TUBES - PART 2: PAEDIATRIC TUBES |
BS EN ISO 5840:2009
|
Cardiovascular implants. Cardiac valve prostheses |
BS EN ISO 5366-1:2004
|
Anaesthetic and respiratory equipment. Tracheostomy tubes Tubes and connectors for use in adults |
BS EN ISO 22794:2009
|
Dentistry. Implantable materials for bone filling and augmentation in oral and maxillofacial surgery. Contents of a technical file |
ISO 5366-1:2000
|
Anaesthetic and respiratory equipment Tracheostomy tubes Part 1: Tubes and connectors for use in adults |
EN 1820:2005+A1:2009
|
Anaesthetic reservoir bags (ISO 5362:2000, modified) |
EN ISO 22803:2005
|
Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
EN ISO 9360-1:2009
|
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (ISO 9360-1:2000) |
CSA Z17664 : 2006
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
CSA Z17664 : 2006 (R2016)
|
STERILIZATION OF MEDICAL DEVICES - INFORMATION TO BE PROVIDED BY THE MANUFACTURER FOR THE PROCESSING OF RESTERILIZABLE MEDICAL DEVICES |
14/30281557 DC : 0
|
BS EN ISO 7198 - CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR PROSTHESES - TUBULAR VASCULAR GRAFTS AND VASCULAR PATCHES |
PD CEN ISO/TR 14969:2005
|
Medical devices. Quality management systems. Guidance on the application of ISO 13485:2003 |
04/30048301 DC : DRAFT MAY 2004
|
BS EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
04/19975667 DC : 0
|
BS ISO 15676 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - SINGLE - USE TUBING PACKS FOR CARDIOPULMONARY BYPASS AND EXTRACORPOREAL MEMBRANCE OXYGENATION |
02/560790 DC : DRAFT FEB 2002
|
BS EN ISO 16671 - OPHTHALMIC IMPLANTS - IRRIGATING SOLUTIONS FOR OPHTHALMIC SURGERY |
CSA Z9360.1 : 2007 : R2012
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - HEAT AND MOISTURE EXCHANGERS (HMES) FOR HUMIDIFYING RESPIRED GASES IN HUMANS - PART 1: HMES FOR USE WITH MINIMUM TIDAL VOLUMES OF 250 ML |
CSA ISO TR 14969 : 2005 : R2010
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
05/30060678 DC : DRAFT SEP 2005
|
BS EN ISO 22794 - DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
CSA ISO 5367 : 2014
|
BREATHING TUBES INTENDED FOR USE WITH ANAESTHETIC APPARATUS AND VENTILATORS |
CAN/CSA-Z9360-1-07 (R2017)
|
Anaesthetic and Respiratory Equipment - Heat and Moisture Exchangers (HMEs) for Humidifying Respired Gases in Humans - Part 1: HMEs for Use with Minimum Tidal Volumes of 250 ml (Adopted ISO 9360-1:2000, first edition, 2000-03-15, with Canadian deviations) |
DIN EN ISO 23328-2 E : 2009
|
BREATHING SYSTEM FILTERS FOR ANAESTHETIC AND RESPIRATORY USE - PART 2: NON-FILTRATION ASPECTS |
CSA Z5361 : 2003
|
ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEAL TUBES AND CONNECTORS |
NF EN ISO 23328-2 : 2009
|
BREATHING SYSTEM FILTERS FOR ANAESTHETIC AND RESPIRATORY USE - PART 2: NON-FILTRATION ASPECTS |
BS EN ISO 9360-2:2009
|
Anaesthetic and respiratory equipment. Heat and moisture exchangers (HMEs) for humidifying respired gases in humans HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml |
BS EN 868-1:1997
|
Packaging materials and systems for medical devices which are to be sterilized General requirements and test methods |
ISO 22803:2004
|
Dentistry — Membrane materials for guided tissue regeneration in oral and maxillofacial surgery — Contents of a technical file |
BS EN 13503-6:2002
|
Ophthalmic implants. Intraocular lenses Shelf-life and transport stability |
DIN EN ISO 5840:2009-08
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES |
DIN EN ISO 9360-1:2009-09
|
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (ISO 9360-1:2000) |
EN ISO 5840:2009
|
Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005) |
DIN EN ISO 9360-2:2009-09
|
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001) |
DIN EN 1282-2:2009-12
|
TRACHEOSTOMY TUBES - PART 2: PAEDIATRIC TUBES |