BS 1263-2(1989) : 1990 AMD 8542
|
REUSABLE HYPODERMIC SYRINGES FOR MEDICAL USE - SPECIFICATION FOR DESIGN AND PERFORMANCE OF ALL GLASS AND METAL AND GLASS SYRINGES |
CSA Z8835.3 : 2008
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
DIN EN ISO 3826-4 E : 2015
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 4: APHERESIS BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES (ISO 3826-4:2015) |
AAMI RD17 : 2007
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - EXTRACORPOREAL BLOOD CIRCUIT FOR HEMODIALYZERS, HEMODIAFILTERS AND HEMOFILTERS |
NF ISO 28620 : 2010
|
MEDICAL DEVICES - NON-ELECTRICALLY DRIVEN PORTABLE INFUSION DEVICES |
10/30212297 DC : 0
|
BS ISO 11040-6 - PREFILLED SYRINGES - PART 6: PLASTIC BARRELS FOR INJECTABLES |
13/30283691 DC : 0
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED |
13/30273308 DC : 0
|
BS EN ISO 3826-4 - PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 4: APHAERESIS BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES |
08/30184486 DC : DRAFT JUNE 2008
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
I.S. EN 1283:1996
|
HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS, HAEMOCONCENTRATORS AND THEIR EXTRACORPOREAL CIRCUITS |
13/30276989 DC : 0
|
BS EN ISO 11070 - STERILE, SINGLE-USE INTRAVASCULAR CATHETER INTRODUCERS |
14/30298693 DC : 0
|
BS ISO 18250-8 - CONNECTORS FOR RESERVOIR DELIVERY SYSTEMS FOR HEALTHCARE APPLICATIONS - PART 8: CITRATE-BASED ANTICOAGULANT SOLUTION FOR APHERESIS APPLICATIONS |
04/30099768 DC : DRAFT DEC 2004
|
PREN ISO 8835-3 - INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: ANAESTHETIC GAS SCAVENGING SYSTEMS - TRANSFER AND RECEIVING SYSTEMS |
16/30331650 DC : 0
|
BS EN ISO 8637-1 - EXTRACORPOREAL SYSTEMS FOR BLOOD PURIFICATION - PART 1: HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
I.S. EN ISO 1135-5:2015
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
DIN EN ISO 1135-3:2014-12 (Draft)
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
02/564514 DC : DRAFT OCT 2002
|
BS EN ISO 8536-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
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 |
02/564515 DC : DRAFT OCT 2002
|
BS EN ISO 8536-8 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 8: INFUSION SETS FOR USE WITH PRESSURE INFUSION EQUIPMENT |
DIN EN ISO 8835-3:2011-02
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
DIN EN ISO 3826-4:2015-12
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 4: APHAERESIS BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES (ISO 3826-4:2015) |
DIN EN ISO 8638:2014-03
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010) |
08/30170025 DC : DRAFT AUG 2008
|
BS ISO 28620 - MEDICAL DEVICES - NON-ELECTRICALLY DRIVEN PORTABLE INFUSION DEVICES |
ISO 8536-12:2007
|
Infusion equipment for medical use Part 12: Check valves |
13/30284721 DC : 0
|
BS EN ISO 8536-8 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 8: INFUSION EQUIPMENT FOR USE WITH PRESSURE INFUSION APPARATUS |
BS EN ISO 8638:2014
|
Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters |
DIN EN ISO 8638 E : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010) |
BS 3930-1(1987) : AMD 8072
|
CONICAL FITTINGS WITH A 6% (LUER) TAPER FOR SYRINGES, NEEDLES AND OTHER MEDICAL EQUIPMENT - SPECIFICATION FOR GENERAL REQUIREMENTS |
06/30153337 DC : DRAFT JULY 2006
|
BS EN 15546-1 - SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
ANSI/AAMI/ISO 25539-1:2017
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES |
I.S. EN ISO 10555-1:2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 1: GENERAL REQUIREMENTS (ISO 10555-1:2013/AMD 1:2017) |
02/565247 DC : DRAFT DEC 2002
|
ISO 8637 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
BS ISO 14972:1998
|
Sterile obturators for single use with over-needle peripheral intravascular catheters |
NF EN 80601-2-30 : 2011 AMD 1 2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
CSA ISO 8637 : 2012
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
EN ISO 22413:2013
|
Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
CSA ISO 8637 : 2012 : R2017
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
DIN EN ISO 7199:2015-06 (Draft)
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) (ISO 7199:2016) |
AAMI HE75 : 2009(R2013)
|
HUMAN FACTORS ENGINEERING - DESIGN OF MEDICAL DEVICES |
I.S. EN ISO 81060-1:2012
|
NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE (ISO 81060-1:2007) |
CSA ISO 7199 : 0
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) |
I.S. EN ISO 22413:2013
|
TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS (ISO 22413:2010) |
ANSI/AAMI/ISO 15674:2016
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HARD-SHELL CARDIOTOMY/VENOUS RESERVOIR SYSTEMS (WITH/WITHOUT FILTER) AND SOFT VENOUS RESERVOIR BAGS |
BS EN ISO 80601-2-12:2011
|
Medical electrical equipment Particular requirements for basic safety and essential performance of critical care ventilators |
UNE-EN ISO 1135-3:2017
|
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
DIN EN ISO 11070:2015-03
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014) |
ISO 15675:2016
|
Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters |
EN ISO 8536-4:2013/A1:2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010/AMD 1:2013) |
BS EN ISO 80601-2-13:2012+A2:2019
|
Medical electrical equipment Particular requirements for basic safety and essential performance of an anaesthetic workstation |
DIN EN ISO 10555-4:2013-11
|
Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2013) |
ONORM EN ISO 22413 : SEP 2013
|
TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS (ISO 22413:2010) |
BS EN ISO 8536-9:2015
|
Infusion equipment for medical use Fluid lines for single use with pressure infusion equipment |
ISO 81060-1:2007
|
Non-invasive sphygmomanometers — Part 1: Requirements and test methods for non-automated measurement type |
ISO 8637:2010
|
Cardiovascular implants and extracorporeal systems Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators |
ISO 8638:2010
|
Cardiovascular implants and extracorporeal systems Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters |
I.S. EN ISO 10555-4:2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 4: BALLOON DILATATION CATHETERS (ISO 10555-4:2013) |
I.S. EN ISO 8536-9:2015
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-9:2015) |
EN ISO 8638:2014
|
Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010) |
EN ISO 80601-2-13:2012
|
Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation (ISO 80601-2-13:2011) |
EN 60601-2-16:2015
|
Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
EN 1283 : 1996
|
HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS, HAEMOCONCENTRATORS AND THEIR EXTRACORPOREAL CIRCUITS |
EN ISO 21647:2009
|
Medical electrical equipment - Particular requirements for the basic safety and essential performance of respiratory gas monitors (ISO 21647:2004, including Cor 1:2005) |
BS EN ISO 80601-2-13:2012
|
Medical electrical equipment Particular requirements for basic safety and essential performance of an anaesthetic workstation |
ISO 13960:2010
|
Cardiovascular implants and extracorporeal systems Plasmafilters |
06/30160058 DC : 0
|
BS EN ISO 8536-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
09/30173644 DC : 0
|
BS EN ISO 80369-1 - SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
14/30296389 DC : 0
|
BS EN ISO 7864 - STERILE HYPODERMIC NEEDLES FOR SINGLE USE - REQUIREMENTS AND TEST METHODS |
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 |
ISO 14972:1998
|
Sterile obturators for single use with over-needle peripheral intravascular catheters |
BS EN ISO 8836:2014
|
Suction catheters for use in the respiratory tract |
BS ISO 8600-1:2015
|
Endoscopes. Medical endoscopes and endotherapy devices General requirements |
06/30159274 DC : 0
|
BS EN 80601-2-30 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED TYPE NON-INVASIVE SPHYGMOMANOMETERS |
CSA Z8638 : 2008
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
ANSI/AAMI/ISO 15675:2016
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - CARDIOPULMONARY BYPASS SYSTEMS - ARTERIAL BLOOD LINE FILTERS |
08/30179586 DC : DRAFT MAR 2008
|
BS ISO 7199 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) |
DIN EN ISO 1135-5:2016-06
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
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) |
AAMI IEC 80601-2-30 : 2009
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
DKD-R 4-1:2018
|
BLOOD PRESSURE TRANSDUCERS |
15/30321715 DC : 0
|
BS ISO 15675 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - CARDIOPULMONARY BYPASS SYSTEMS - ARTERIAL BLOOD LINE FILTERS |
DIN EN ISO 8836 E : 2015
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT (ISO 8836:2014) |
15/30288418 DC : 0
|
BS EN ISO 80369-2 - SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 2: CONNECTORS FOR BREATHING SYSTEMS AND DRIVING GASES APPLICATIONS |
14/30303657 DC : 0
|
BS EN ISO 1135-3 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SET FOR SINGLE USE |
DIN ISO 11040-4 E : 2017
|
PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
13/30284770 DC : 0
|
BS EN ISO 8536-9 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR USE WITH PRESSURE INFUSION EQUIPMENT |
BS EN ISO 7199:2017
|
Cardiovascular implants and artificial organs. Blood-gas exchangers (oxygenators) |
15/30321712 DC : 0
|
BS ISO 15674 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HARD-SHELL CARDIOTOMY/VENOUS RESERVOIR SYSTEMS (WITH/WITHOUT FILTER) AND SOFT VENOUS RESERVOIR BAGS |
15/30321957 DC : 0
|
BS EN ISO 7199 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS BLOOD-GAS EXCHANGERS (OXYGENATORS) |
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 |
DIN EN ISO 1135-5 E : 2016
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
BS ISO 18241:2016
|
Cardiovascular implants and extracorporeal systems. Cardiopulmonary bypass systems. Venous bubble traps |
BS EN 80601-2-30 : 2010
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
BS ISO 15674:2009
|
Cardiovascular implants and artificial organs. Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags |
DIN EN ISO 8836:2015-02
|
Suction catheters for use in the respiratory tract (ISO 8836:2014); German version EN ISO 8836:2014 |
BS ISO 11040-4:2015
|
Prefilled syringes Glass barrels for injectables and sterilized subassembled syringes ready for filling |
08/30179592 DC : DRAFT MAR 2008
|
BS ISO 15675 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - CARDIOPULMONARY BYPASS SYSTEMS - ARTERIAL BLOOD LINE FILTERS |
BS ISO 81060-1 : 2007 COR 2012
|
NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
06/30137313 DC : 0
|
ISO/IEC 81060-1 - NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR MECHANICAL TYPE |
CSA Z8836 :2011
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
DIN EN ISO 81060-1:2012-08
|
Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007) |
CSA Z21647 : 2007 : R2012 : FR
|
MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
CSA ISO 8638 : 2012 : R2017
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
BS EN ISO 10555-1 : 2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 1: GENERAL REQUIREMENTS |
NF ISO 14972 : 1999
|
STERILE OBTURATORS FOR SINGLE USE WITH OVER-NEEDLE PERIPHERAL INTRAVASCULAR CATHETERS |
BS EN ISO 11070 : 2014
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES |
AAMI BP22 : 1994 : R2011
|
BLOOD PRESSURE TRANSDUCERS |
AAMI ISO 8638 : 2010
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HEMODIALYZERS, HEMODIAFILTERS AND HEMOFILTERS |
AAMI IEC 60601-2-16 : 2012
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-16: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HEMODIALYSIS, HEMODIAFILTRATION AND HEMOFILTRATION EQUIPMENT |
AAMI ID54 : 1996 : R2012
|
ENTERAL FEEDING SET ADAPTERS AND CONNECTORS |
AAMI ISO 8836 : 2015
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
AAMI ISO 8638 : 2010 : R2015
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HEMODIALYZERS, HEMODIAFILTERS AND HEMOFILTERS |
UNE-EN ISO 1135-5:2016
|
Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015) |
I.S. EN ISO 11070:2014
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014) |
I.S. EN 60601-2-16:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-16: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HAEMODIALYSIS, HAEMODIAFILTRATION AND HAEMOFILTRATION EQUIPMENT |
ISO 11070:2014
|
Sterile single-use intravascular introducers, dilators and guidewires |
CSA C22.2 No. 80601-2-12 : 2012
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
ASTM D 7458 : 2014 : REDLINE
|
Standard Test Method for Determination of Beryllium in Soil, Rock, Sediment, and Fly Ash Using Ammonium Bifluoride Extraction and Fluorescence Detection |
IEC 80601-2-30:2018
|
Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
ISO 8836:2014
|
Suction catheters for use in the respiratory tract |
DIN EN ISO 1135-4:2016-06
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
DIN EN 20594-1:1995-01
|
CONICAL FITTINGS WITH A 6 % (LUER) TAPER FOR SYRINGES, NEEDLES AND CERTAIN OTHER MEDICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS |
DIN EN ISO 8835-2:2009-08
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 2: ANAESTHETIC BREATHING SYSTEMS |
BS EN ISO 7864:2016
|
Sterile hypodermic needles for single use. Requirements and test methods |
ISO 7886-2:1996
|
Sterile hypodermic syringes for single use Part 2: Syringes for use with power-driven syringe pumps |
UNE-EN ISO 80601-2-13:2013
|
Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation (ISO 80601-2-13:2011) |
BS EN 20594-1:1994
|
Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment General requirements |
UNE-EN ISO 8536-4:2013
|
Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2010) |
BS EN ISO 8835-2:2009
|
Inhalational anaesthesia systems Anaesthetic breathing systems (ISO 8835-2:2007) |
ISO 7199:2016
|
Cardiovascular implants and artificial organs Blood-gas exchangers (oxygenators) |
BS EN ISO 8536-8:2015
|
Infusion equipment for medical use Infusion sets for single use with pressure infusion apparatus |
I.S. EN ISO 8536-11:2015
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 11: INFUSION FILTERS FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-11:2015) |
I.S. EN ISO 8536-10:2015
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 10: ACCESSORIES FOR FLUID LINES FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-10:2015) |
I.S. EN ISO 1135-4:2015
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
ONORM EN ISO 8836 : 2015
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT (ISO 8836:2014) |
I.S. EN ISO 595-2:1995
|
REUSABLE - ALL-GLASS OR METAL-AND-GLASS SYRINGES FOR MEDICAL USE - PART 2: DESIGN, PERFORMANCE REQUIREMENTS AND TESTS |
I.S. EN ISO 8536-8:2015
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 8: INFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 8536-8:2015) |
I.S. EN ISO 7864:2016
|
STERILE HYPODERMIC NEEDLES FOR SINGLE USE - REQUIREMENTS AND TEST METHODS (ISO/DIS 7864:2014) |
BS 5081-1:1994
|
Sterile hypodermic syringes and needles Specification for sterile, single-use hypodermic syringes for manual use |
DIN EN ISO 1135-3:2017-05
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
UNI EN ISO 11070 : 2015
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES |
BS ISO 11040-6:2012
|
Prefilled syringes Plastic barrels for injectables |
UNI EN ISO 81060-1 : 2012
|
NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
16/30339096 DC : 0
|
BS EN ISO 7886-3 - STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
NF EN ISO 8835-3 : 2009 AMD 1 2011
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
DIN EN ISO 7199 E : 2017
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) (ISO 7199:2016) |
BS ISO 15675:2009
|
Cardiovascular implants and artificial organs. Cardiopulmonary bypass systems. Arterial blood line filters |
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) |
I.S. EN ISO 8835-2:2009
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 2: ANAESTHETIC BREATHING SYSTEMS |
BS EN ISO 80369-7:2017
|
Small-bore connectors for liquids and gases in healthcare applications Connectors for intravascular or hypodermic applications |
DIN EN ISO 8637 E : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS (ISO 8637:2010, INCLUDING AMENDMENT 1 2013-04-01) |
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 |
BS EN ISO 81060-1:2012
|
Non-invasive sphygmomanometers Requirements and test methods for non-automated measurement type |
13/30284773 DC : 0
|
BS EN ISO 8536-10 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 10: ACCESSORIES FOR FLUID LINES FOR USE WITH PRESSURE INFUSION EQUIPMENT |
13/30273499 DC : 0
|
BS ISO 11040-4 - PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING |
02/564513 DC : DRAFT OCT 2002
|
BS EN ISO 1135-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
13/30284776 DC : 0
|
BS EN ISO 8536-11 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 11: INFUSION FILTERS FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT |
BS ISO 8536-12 : 2007
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 12: CHECK VALVES |
02/564516 DC : DRAFT OCT 2002
|
BS EN ISO 8536-9 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR USE WITH PRESSURE INFUSION EQUIPMENT |
BS ISO 28620:2010
|
Medical devices. Non-electrically driven portable infusion devices |
11/30235365 DC : 0
|
BS EN ISO 10555-4 - INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 4: BALLOON DILATATION CATHETERS |
AAMI ISO 81060-1:2007(R2013)
|
NON INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
15/30275221 DC : 0
|
BS ISO 18241 - CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - CARDIOPULMONARY BYPASS SYSTEMS - VENOUS BUBBLE TRAPS |
AAMI ID54 : 1996 : R2005
|
ENTERAL FEEDING SET ADAPTERS AND CONNECTORS |
02/564517 DC : DRAFT OCT 2002
|
BS EN ISO 8536-10 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 10: ACCESSORIES FOR FLUID LINES FOR USE WITH PRESSURE INFUSION EQUIPMENT |
11/30228364 DC : 0
|
BS EN ISO 10555-1 - INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 1: GENERAL REQUIREMENTS |
CSA Z8836 : 2011 : FR
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
UNI EN ISO 8836 : 2015
|
A SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
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) |
UNE-EN ISO 8836:2015
|
Suction catheters for use in the respiratory tract (ISO 8836:2014) |
BS EN ISO 8637:2014
|
Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators |
UNE-EN 80369-5:2017
|
Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications |
DIN EN ISO 22413:2013-10
|
Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
CSA ISO 8637 : 2012 : INC : AMD 1 : 2015
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
CSA Z8836 : 2011 : R2015
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT |
I.S. EN ISO 80369-7:2017 COR 2017
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 7: CONNECTORS FOR INTRAVASCULAR OR HYPODERMIC APPLICATIONS (ISO 80369-7:2016, CORRECTED VERSION 2016-12-01) |
CSA C22.2 No. 80601-2-30 : 2010 : INC : COR 1 : 2011
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
CSA C22.2 No. 80601-2-30 : 2010FR
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
ISO 18241:2016
|
Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps |
CSA C22.2 No. 80601-2-30 : 2010 : R2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
I.S. EN ISO 1135-3:2017
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
AAMI HE75 : 2009
|
HUMAN FACTORS ENGINEERING - DESIGN OF MEDICAL DEVICES |
I.S. EN 80601-2-30:2010
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
ANSI/AAMI/ISO 18241:2016
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - CARDIOPULMONARY BYPASS SYSTEMS - VENOUS BUBBLE TRAPS |
ANSI/AAMI/ISO 80369-7:2016
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 7: CONNECTORS FOR INTRAVASCULAR OR HYPODERMIC APPLICATIONS |
I.S. EN ISO 8637:2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS (ISO 8637:2010, INCLUDING AMENDMENT 1 2013-04-01) |
ANSI/AAMI BP22:1994(2016)
|
BLOOD PRESSURE TRANSDUCERS |
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) |
EN ISO 10555-1:2013/A1:2017
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 1: GENERAL REQUIREMENTS (ISO 10555-1:2013/AMD 1:2017) |
AAMI RD16 : 2007
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HEMODIALYZERS, HEMODIAFILTERS, HEMOFILTERS AND HEMOCONCENTRATORS |
I.S. EN ISO 8638:2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010) |
I.S. EN ISO 80601-2-13:2012
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-13: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AN ANAESTHETIC WORKSTATION (ISO 80601-2-13:2011) |
CSA Z8835.2 : 2008
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 2: ANAESTHETIC BREATHING SYSTEMS FOR ADULTS |
UNI EN ISO 8637 : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
ISO 595-2:1987
|
Reusable all-glass or metal-and-glass syringes for medical use Part 2: Design, performance requirements and tests |
I.S. EN ISO 8836:2014
|
SUCTION CATHETERS FOR USE IN THE RESPIRATORY TRACT (ISO 8836:2014) |
DIN EN ISO 8536-10:2015-11
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 10: ACCESSORIES FOR FLUID LINES FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-10:2015) |
DIN EN ISO 8536-9:2015-11
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-9:2015) |
BS EN ISO 8536-10:2015
|
Infusion equipment for medical use Accessories for fluid lines for single use with pressure infusion equipment |
BS EN ISO 10555-4:2013
|
Intravascular catheters. Sterile and single-use catheters Balloon dilatation catheters |
ISO 1135-5:2015
|
Transfusion equipment for medical use — Part 5: Transfusion sets for single use with pressure infusion apparatus |
ISO 8835-2:2007
|
Inhalational anaesthesia systems Part 2: Anaesthetic breathing systems |
ISO 8835-3:2007
|
Inhalational anaesthesia systems Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems |
UNI EN ISO 8536-4 : 2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
BS EN 60601-2-16:2015
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
BS EN ISO 1135-4:2015
|
Transfusion equipment for medical use Transfusion sets for single use, gravity feed |
UNE-EN ISO 8536-8:2015
|
Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus (ISO 8536-8:2015) |
EN ISO 8836:2014
|
Suction catheters for use in the respiratory tract (ISO 8836:2014) |
CSA C22.2 No. 80601-2-12 : 2012(R2017)
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
EN ISO 3826-4:2015
|
Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015) |
EN ISO 8536-9:2015
|
Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (ISO 8536-9:2015) |
UNI EN ISO 21647 : 2009
|
MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
UNI EN ISO 10555-4 : 2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 4: BALLOON DILATATION CATHETERS |
DIN EN ISO 8637:2014-03
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS (ISO 8637:2010, INCLUDING AMENDMENT 1:2013-04-01) |
BS EN ISO 25539-1:2017
|
Cardiovascular implants. Endovascular devices Endovascular prostheses |
AAMI ISO 81060-1 : 2007
|
NON INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
01/561789 DC : DRAFT APR 2001
|
BS ISO 13960 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - PLASMAFILTERS |
I.S. EN ISO 21647:2009
|
MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
UNI EN ISO 8835-2 : 2009
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 2: ANAESTHETIC BREATHING SYSTEMS |
16/30331656 DC : 0
|
BS ISO 8637-3 - EXTRACORPOREAL SYSTEMS FOR BLOOD PURIFICATION - PART 3: PLASMAFILTERS |
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 |
07/30147572 DC : DRAFT SEP 2007
|
BS ISO 27427 - ANAESTHETIC AND RESPIRATORY EQUIPMENT - NEBULIZING SYSTEMS AND COMPONENTS |
BS ISO 7886-2 : 1996 AMD 9835
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - SYRINGES FOR USE WITH POWER-DRIVEN SYRINGE PUMPS |
15/30289037 DC : 0
|
BS EN ISO 7886-1 - STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 1: SYRINGES FOR MANUAL USE |
DIN EN ISO 1135-3 E : 2017
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
AAMI ISO 8637 : 2010
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HEMODIALYZERS, HEMODIAFILTERS, HEMOFILTERS AND HEMOCONCENTRATORS |
BS EN ISO 3826-4:2015
|
Plastics collapsible containers for human blood and blood components Aphaeresis blood bag systems with integrated features |
DIN 254:2003-04
|
GEOMETRICAL PRODUCT SPECIFICATIONS (GPS) - SERIES OF CONICAL TAPERS AND TAPER ANGLES - VALUES FOR SETTING TAPER ANGLES AND SETTING HEIGHTS |
UNI EN ISO 8835-3 : 2010
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
BS 1263-1:1989
|
Reusable hypodermic syringes for medical use. Specification for dimensions of all-glass and metal-and-glass syringes |
16/30331653 DC : 0
|
BS EN ISO 8637-2 - EXTRACORPOREAL SYSTEMS FOR BLOOD PURIFICATION - PART 2: EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
BS EN ISO 22413:2013
|
Transfer sets for pharmaceutical preparations. Requirements and test methods |
02/565260 DC : DRAFT DEC 2002
|
ISO 8638 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
16/30346835 DC : 0
|
BS ISO 20789 - ANAESTHETIC AND RESPIRATORY EQUIPMENT - PASSIVE HUMIDIFIERS |
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 |
02/564518 DC : DRAFT OCT 2002
|
BS EN ISO 8536-11 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 11: INFUSION FILTERS FOR USE WITH PRESSURE INFUSION EQUIPMENT |
DIN 13098-1:1992-05
|
SINGLE USE PLASTICS SYRINGES FOR MEDICAL PURPOSES - SINGLE USE PLASTICS SYRINGES FOR GENERAL USE - DIMENSIONS, REQUIREMENTS, TEST |
CSA Z21647:2007
|
MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
PREN ISO 80369-1 : DRAFT 2009
|
SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 1: GENERAL REQUIREMENTS |
UNI EN ISO 8638 : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
CEI EN 60601-2-16 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-16: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HAEMODIALYSIS, HAEMODIAFILTRATION AND HAEMOFILTRATION EQUIPMENT |
I.S. EN ISO 25539-1:2017
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |
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) |
I.S. EN 80369-5:2016
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 5: CONNECTORS FOR LIMB CUFF INFLATION APPLICATIONS |
ISO 15674:2016
|
Cardiovascular implants and artificial organs — Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags |
ISO 11040-4:2015
|
Prefilled syringes Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling |
EN ISO 8637:2014
|
Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01) |
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 |
I.S. EN ISO 8536-4:2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010) |
BS EN ISO 8536-4 : 2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
DIN EN ISO 8536-11:2015-11
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 11: INFUSION FILTERS FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-11:2015) |
DIN EN ISO 8536-4:2013-07
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013) |
UNE-EN ISO 1135-4:2016
|
Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015) |
BS EN ISO 7886-2:1997
|
Sterile hypodermic syringes for single use Syringes for use with power-driven syringe pumps |
ISO 10555-4:2013
|
Intravascular catheters — Sterile and single-use catheters — Part 4: Balloon dilatation catheters |
ISO 8536-10:2015
|
Infusion equipment for medical use Part 10: Accessories for fluid lines for single use with pressure infusion equipment |
ISO 1135-3:2016
|
Transfusion equipment for medical use Part 3: Blood-taking sets for single use |
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 1135-4:2015
|
Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
UNE-EN ISO 8536-10:2015
|
Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment (ISO 8536-10:2015) |
UNE-EN ISO 22413:2013
|
Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
ISO 7864:2016
|
Sterile hypodermic needles for single use — Requirements and test methods |
ISO 8536-8:2015
|
Infusion equipment for medical use Part 8: Infusion sets for single use with pressure infusion apparatus |
ISO 8536-9:2015
|
Infusion equipment for medical use Part 9: Fluid lines for single use with pressure infusion equipment |
ISO 8536-4:2010
|
Infusion equipment for medical use Part 4: Infusion sets for single use, gravity feed |
ISO 80601-2-13:2011
|
Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
UNE-EN ISO 11070:2015
|
Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014) |
EN ISO 7886-2 : 1997
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - SYRINGES FOR USE WITH POWER-DRIVEN SYRINGE PUMPS |
ISO 8536-11:2015
|
Infusion equipment for medical use Part 11: Infusion filters for single use with pressure infusion equipment |
ISO 21647:2004
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of respiratory gas monitors |
ISO 594-1:1986
|
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements |
UNE-EN ISO 7864:2017
|
Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016) |
UNI EN ISO 80601-2-13 : 2013
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-13: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AN ANAESTHETIC WORKSTATION |
BS EN 30-1-2:2012
|
Domestic cooking appliances burning gas. Safety Appliances having forced-convection ovens and/or grills |
DIN EN 80369-5:2017-10
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 5: CONNECTORS FOR LIMB CUFF INFLATION APPLICATIONS (IEC 80369-5:2016 + COR.1:2017) |
EN 30-1-2:2012
|
Domestic cooking appliances burning gas - Safety - Part 1-2: Appliances having forced-convection ovens and/or grills |
EN ISO 1135-3:2017
|
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
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 20594-1:1993/A1:1997
|
CONICAL FITTINGS WITH A 6% (LUER) TAPER FOR SYRINGES, NEEDLES AND CERTAIN OTHER MEDICAL EQUIPMENT - GENERAL REQUIREMENTS |
IEC 80601-2-30:2018 RLV
|
Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
EN ISO 8536-10:2015
|
Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment (ISO 8536-10:2015) |
EN ISO 8536-8:2015
|
Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus (ISO 8536-8:2015) |
EN ISO 7864:2016
|
Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016) |
EN ISO 8835-3:2009/A1:2010
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
EN ISO 8536-11:2015
|
Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment (ISO 8536-11:2015) |
EN ISO 595-2:1994
|
REUSABLE ALL-GLASS OR METAL-AND-GLASS SYRINGES FOR MEDICAL USE - PART 2: DESIGN, PERFORMANCE REQUIREMENTS AND TESTS |
EN ISO 1135-5:2015
|
Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015) |
EN ISO 10555-4:2013
|
Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2013) |
EN ISO 8835-2:2009
|
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems (ISO 8835-2:2007) |
ONORM EN ISO 11070 : 2015
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014) |
DIN EN 80369-5 E : 2017
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 5: CONNECTORS FOR LIMB CUFF INFLATION APPLICATIONS (IEC 80369-5:2016 + COR.1:2017) |
12/30228200 DC : 0
|
BS ISO 8600-1 - ENDOSCOPES - MEDICAL ENDOSCOPES AND ENDOTHERAPY DEVICES - PART 1: GENERAL REQUIREMENTS |
BS EN ISO 8835-3 : 2009
|
INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
BS EN ISO 1135-5:2015
|
Transfusion equipment for medical use Transfusion sets for single use with pressure infusion apparatus |
BS EN ISO 1135-3:2017
|
Transfusion equipment for medical use Blood-taking sets for single use |
UNE-EN ISO 80369-7:2017
|
Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01) |
13/30255554 DC : 0
|
BS EN ISO 80369-7 - SMALL BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 7: CONNECTORS WITH 6% (LUER) TAPER FOR INTRAVASCULAR OR HYPODERMIC APPLICATIONS |
EN ISO 80369-7:2017
|
Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01) |
ANSI/AAMI/ISO 80369-5:2016
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 5: CONNECTORS FOR LIMB CUFF INFLATION APPLICATIONS |
AAMI ISO 7199 : 2009
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) |
ISO 11040-6:2012
|
Prefilled syringes Part 6: Plastic barrels for injectables |
CSA Z8637 : 2008
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
DIN EN ISO 80369-7 E : 2017
|
SMALL-BORE CONNECTORS FOR LIQUIDS AND GASES IN HEALTHCARE APPLICATIONS - PART 7: CONNECTORS FOR INTRAVASCULAR OR HYPODERMIC APPLICATIONS (ISO 80369-7:2016, CORRECTED VERSION 2016-12-01) |
08/30179589 DC : DRAFT MAR 2008
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BS ISO 15674 - CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - HARD-SHELL CARDIOTOMY/VENOUS RESERVOIR SYSTEMS (WITH/WITHOUT FILTER) AND SOFT VENOUS RESERVOIR BAGS |
DIN ISO 8536-12:2013-04
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Infusion equipment for medical use - Part 12: Check valves (ISO 8536-12:2007 + Amd. 1:2012) |
DIN ISO 11040-4:2007-10
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PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
CSA ISO 8638 : 2012
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
BS ISO 22413:2010
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Transfer sets for pharmaceutical preparations. Requirements and test methods |
13/30283694 DC : 0
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BS EN ISO 1135-5 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS |
I.S. EN ISO 3826-4:2015
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PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 4: APHAERESIS BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES (ISO 3826-4:2015) |
IEC 80601-2-30 REDLINE : 2ED 2018
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
CSA ISO 8637 : 2012 : INC : AMD 1 : 2015 : R2017
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS |
CSA Z21647 : 2007 : R2012
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MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
CSA C22.2 No. 60601.2.16 : 2014(R2019)
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-16: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HAEMODIALYSIS, HAEMODIAFILTRATION AND HAEMOFILTRATION EQUIPMENT |
BS ISO 7199 : 2009
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CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) |
I.S. EN ISO 8835-3:2009
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INHALATIONAL ANAESTHESIA SYSTEMS - PART 3: TRANSFER AND RECEIVING SYSTEMS OF ACTIVE ANAESTHETIC GAS SCAVENGING SYSTEMS |
ISO 10555-1:2013
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Intravascular catheters — Sterile and single-use catheters — Part 1: General requirements |
I.S. EN ISO 7199:2017
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CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) (ISO 7199:2016) |
ISO 28620:2010
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Medical devices Non-electrically driven portable infusion devices |
ISO 8600-1:2015
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Endoscopes — Medical endoscopes and endotherapy devices — Part 1: General requirements |
DIN EN ISO 8536-8:2015-11
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 8: INFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 8536-8:2015) |
UNE-EN ISO 8536-11:2015
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Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment (ISO 8536-11:2015) |
UNE-EN ISO 8536-9:2015
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Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (ISO 8536-9:2015) |
ISO 22413:2010
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Transfer sets for pharmaceutical preparations Requirements and test methods |
ISO 25539-1:2017
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Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses |
BS EN ISO 8536-11:2015
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Infusion equipment for medical use Infusion filters for single use with pressure infusion equipment |
UNE-EN ISO 10555-4:2014
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Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2013) |
BS EN ISO 21647:2009
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Medical electrical equipment. Particular requirements for the basic safety and essential performance of respiratory gas monitors |
EN ISO 7199:2017
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Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2016) |
ISO 3826-4:2015
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Plastics collapsible containers for human blood and blood components — Part 4: Aphaeresis blood bag systems with integrated features |
DIN EN ISO 80369-7:2017-10
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Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01) |
EN ISO 81060-1:2012
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Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007) |
EN ISO 1135-4 : 2015 COR 2016
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TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
UNI EN ISO 22413 : 2013
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TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS |
EN 80601-2-30:2010/A1:2015
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS (IEC 80601-2-30:2009/A1:2013) |
DIN ISO 11040-4:2017-07
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PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
ONORM EN ISO 10555-4 : 2013
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INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 4: BALLOON DILATATION CATHETERS (ISO 10555-4:2013) |