AAMI RD17 : 2007
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - EXTRACORPOREAL BLOOD CIRCUIT FOR HEMODIALYZERS, HEMODIAFILTERS AND HEMOFILTERS |
13/30283691 DC : 0
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED |
BS EN ISO 1135-5:2015
|
Transfusion equipment for medical use Transfusion sets for single use with pressure infusion apparatus |
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 |
03/113406 DC : DRAFT OCT 2003
|
ISO 7886-3 - STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED DOSE IMMUNIZATION |
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 |
I.S. EN ISO 10555-6:2017
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
14/30298393 DC : 0
|
BS EN ISO 6009 - HYPODERMIC NEEDLES FOR SINGLE USE - COLOUR CODING FOR IDENTIFICATION |
DIN EN ISO 8638:2014-03
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010) |
12/30266576 DC : 0
|
BS EN 13718-2 - MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS OF AIR AMBULANCES |
BS EN ISO 8638:2014
|
Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters |
17/30350521 DC : 0
|
BS EN ISO 7886-4 - STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
DIN EN ISO 8638 E : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010) |
AAMI ID26:2004
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFUSION PUMPS AND CONTROLLERS |
AAMI ID26 : 2004 : R2013
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFUSION PUMPS AND CONTROLLERS |
EN ISO 7886-4:2009
|
Sterile hypodermic syringes for single use - Part 4: Syringes with re-use prevention feature (ISO 7886-4:2006) |
EN ISO 22413:2013
|
Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
CAN/CSA-Z316.6:2014(R2019)
|
Sharps injury protection - Requirements and test methods - Sharps containers (Adopted ISO 23907:2012, first edition, 2012-09-01, with Canadian deviations) |
I.S. EN ISO 22413:2013
|
TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS (ISO 22413:2010) |
I.S. EN ISO 8871-5:2016
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
ASTM F 2132 : 2001
|
Standard Specification for Puncture Resistance of Materials Used in Containers for Discarded Medical Needles and Other Sharps |
UNE-EN ISO 1135-3:2017
|
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
UNI EN ISO 7886-4 : 2009
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
DIN EN ISO 10555-6:2017-11
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
PD 6632:1998
|
Biotechnology. Laboratories for research, development and analysis. Guidance on the selection of equipment needed for biotechnology laboratories according to the degree of hazard |
DIN EN ISO 11070:2015-03
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014) |
ASTM F 2132 : 2001 : R2008
|
Standard Specification for Puncture Resistance of Materials Used in Containers for Discarded Medical Needles and Other Sharps |
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) |
EN 13718-2:2015
|
Medical vehicles and their equipment - Air ambulances - Part 2: Operational and technical requirements for air ambulances |
BS EN ISO 8536-9:2015
|
Infusion equipment for medical use Fluid lines for single use with pressure infusion equipment |
ISO 23907:2012
|
Sharps injury protection Requirements and test methods Sharps containers |
ISO 10555-5:2013
|
Intravascular catheters — Sterile and single-use catheters — Part 5: Over-needle peripheral catheters |
BS EN ISO 7885:2010
|
Dentistry. Sterile injection needles for single use |
ISO 8638:2010
|
Cardiovascular implants and extracorporeal systems Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters |
ISO 8871-5:2016
|
Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing |
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) |
DIN EN ISO 7886-4:2010-01
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
EN ISO 8638:2014
|
Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010) |
EN 1283 : 1996
|
HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS, HAEMOCONCENTRATORS AND THEIR EXTRACORPOREAL CIRCUITS |
NF EN ISO 11608-2 : 2012
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES |
13/30261812 DC : 0
|
BS ISO 10555-6 - INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS |
DIN EN ISO 8871-5 E : 2017
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
CSA Z8638 : 2008
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
BS EN ISO 23907:2012
|
Sharps injury protection. Requirements and test methods. Sharps containers |
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) |
I.S. EN ISO 23907:2012
|
SHARPS INJURY PROTECTION - REQUIREMENTS AND TEST METHODS - SHARPS CONTAINERS (ISO 23907:2012) |
CEI EN 60664-4 : 2006
|
INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 4: CONSIDERATION OF HIGH-FREQUENCY VOLTAGE STRESS |
17/30357741 DC : 0
|
BS ISO 11040-6 - PREFILLED SYRINGES - PART 6: PLASTIC BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING |
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) |
DIN EN ISO 23907:2013-01
|
SHARPS INJURY PROTECTION - REQUIREMENTS AND TEST METHODS - SHARPS CONTAINERS (ISO 23907:2012) |
15/30324254 DC : 0
|
BS EN ISO 8871-5 - ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING |
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) |
14/30294895 DC : 0
|
BS EN ISO 8537 - STERILE SINGLE-USE SYRINGES, WITH OR WITHOUT NEEDLE, FOR INSULIN |
09/30168835 DC : 0
|
BS EN ISO 7885 - STERILE DENTAL INJECTION NEEDLES FOR SINGLE USE |
BS ISO 11040-4:2015
|
Prefilled syringes Glass barrels for injectables and sterilized subassembled syringes ready for filling |
CSA ISO 8638 : 2012 : R2017
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
UNE-EN 13976-2:2011
|
Rescue systems - Transportation of incubators - Part 2: System requirements |
BS EN ISO 11070 : 2014
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES |
AAMI ISO 8638 : 2010
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HEMODIALYZERS, HEMODIAFILTERS AND HEMOFILTERS |
ANSI/AAMI/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 |
I.S. EN 60601-2-24:2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-24: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF INFUSION PUMPS AND CONTROLLERS |
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) |
ISO 11040-8:2016
|
Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes |
BS EN ISO 7886-4:2009
|
Sterile hypodermic syringes for single use Syringes with re-use prevention feature |
I.S. EN 60664-4:2006
|
INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 4: CONSIDERATION OF HIGH-FREQUENCY VOLTAGE STRESS |
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) |
UNE-EN ISO 11608-3:2013
|
Needle-based injection systems for medical use - Requirements and test methods - Part 3: Finished containers (ISO 11608-3:2012) |
BS EN ISO 7886-3:2009
|
Sterile hypodermic syringes for single use Auto-disable syringes for fixed-dose immunization |
ISO 7886-2:1996
|
Sterile hypodermic syringes for single use Part 2: Syringes for use with power-driven syringe pumps |
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 6009 : 1995
|
HYPODERMIC NEEDLES FOR SINGLE USE - COLOUR CODING FOR IDENTIFICATION |
IEC 60664-4:2005
|
Insulation coordination for equipment within low-voltage systems - Part 4: Consideration of high-frequency voltage stress |
DIN EN ISO 7886-3:2010-01
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
I.S. EN ISO 6009:2016
|
HYPODERMIC NEEDLES FOR SINGLE USE - COLOUR CODING FOR IDENTIFICATION (ISO/DIS 6009:2014) |
UNI EN ISO 7886-3 : 2009
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
I.S. EN ISO 10555-5:2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 5: OVER-NEEDLE PERIPHERAL CATHETERS (ISO 10555-5:2013) |
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) |
DIN EN ISO 7885:2010-06
|
Dentistry - Sterile injection needles for single use (ISO 7885:2010) |
I.S. EN ISO 8537:2016
|
STERILE SINGLE-USE SYRINGES, WITH OR WITHOUT NEEDLE, FOR INSULIN (ISO 8537:2016) |
I.S. EN ISO 11608-3:2012
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 3: FINISHED CONTAINERS (ISO 11608-3:2012) |
I.S. EN ISO 11608-2:2012
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES (ISO 11608-2:2012) |
I.S. EN ISO 7885:2010
|
DENTISTRY - STERILE INJECTION NEEDLES FOR SINGLE 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 |
16/30339096 DC : 0
|
BS EN ISO 7886-3 - STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
DIN EN ISO 10555-6 E : 2017
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
BS ISO 17218:2014
|
Sterile acupuncture needles for single use |
PD ISO/TR 19244:2014
|
Guidance on transition periods for standards developed by ISO/TC 84. Devices for administration of medicinal products and catheters |
CEI EN 60601-2-24 : 2016
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-24: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF INFUSION PUMPS AND CONTROLLERS |
ASTM F 2132 : 2001 : R2008 : EDT 1
|
Standard Specification for Puncture Resistance of Materials Used in Containers for Discarded Medical Needles and Other Sharps (Withdrawn 2017) |
BS ISO 10555-6 : 2015
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS |
PREN ISO 11608-2 : DRAFT 2010
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES |
13/30273499 DC : 0
|
BS ISO 11040-4 - PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING |
13/30284770 DC : 0
|
BS EN ISO 8536-9 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR USE WITH PRESSURE INFUSION EQUIPMENT |
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 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 |
10/30209606 DC : 0
|
BS EN ISO 23907 - SHARPS INJURY PROTECTION - REQUIREMENTS AND TEST METHODS - SHARPS CONTAINERS |
EN ISO 10555-6:2017
|
Intravascular catheters - Sterile and single-use catheters - Part 6: Subcutaneous implanted ports (ISO 10555-6:2015) |
AAMI ID26 : 2004 : R2009
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFUSION PUMPS AND CONTROLLERS |
DIN EN ISO 22413:2013-10
|
Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
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 |
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 11070:2014
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014) |
DIN EN ISO 7886-4 E : 2010
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
BS EN ISO 10555-6:2017
|
Intravascular catheters. Sterile and single-use catheters Subcutaneous implanted ports |
ISO 7886-4:2006
|
Sterile hypodermic syringes for single use Part 4: Syringes with re-use prevention feature |
ISO 10555-6:2015
|
Intravascular catheters Sterile and single-use catheters Part 6: Subcutaneous implanted ports |
DIN EN ISO 7886-3 E : 2010
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
DIN EN ISO 11608-3 E : 2013
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 3: FINISHED CONTAINERS (ISO 11608-3:2012) |
DIN EN 13718-2:2015-05
|
MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES |
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) |
ISO 1135-5:2015
|
Transfusion equipment for medical use — Part 5: Transfusion sets for single use with pressure infusion apparatus |
UNI EN ISO 8536-4 : 2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
UNE-EN ISO 10555-5:2014
|
Intravascular catheters - Sterile and single-use catheters - Part 5: Over-needle peripheral catheters (ISO 10555-5:2013) |
UNE-EN 13718-2:2015
|
Medical vehicles and their equipment - Air ambulances - Part 2: Operational and technical requirements for air ambulances |
BS EN ISO 1135-4:2015
|
Transfusion equipment for medical use Transfusion sets for single use, gravity feed |
EN ISO 7886-3:2009
|
Sterile hypodermic syringes for single use - Part 3: Auto-disable syringes for fixed-dose immunization (ISO 7886-3:2005) |
I.S. EN ISO 7886-3:2009
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
UNE-EN ISO 7885:2010
|
Dentistry - Sterile injection needles for single use (ISO 7885:2010) |
ONORM EN 13718-2 : 2015
|
MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES |
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 10555-5 : 2013
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 5: OVER-NEEDLE PERIPHERAL CATHETERS |
UNI EN ISO 11608-2 : 2012
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES |
UNI EN ISO 11608-3 : 2013
|
NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 3: FINISHED CONTAINERS |
UNI EN ISO 7885 : 2010
|
DENTISTRY - STERILE INJECTION NEEDLES FOR SINGLE USE |
CSA C22.2 No. 60601.2.24 : 2015
|
MEDICAL ELECTRICAL EQUIPMENT - PART 2-24: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF INFUSION PUMPS AND CONTROLLERS |
15/30282343 DC : 0
|
BS ISO 18746 - TRADITIONAL CHINESE MEDICINE - INTRADERMAL ACUPUNCTURE NEEDLES |
PREN 13976-2 : DRAFT 2016
|
RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
08/30184486 DC : DRAFT JUNE 2008
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
UNI EN 13976-2 : 2011
|
RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
15/30304642 DC : 0
|
BS ISO 11040-8 - PREFILLED SYRINGES - PART 8: REQUIREMENTS AND TEST METHODS FOR FINISHED PRIFILLED SYRINGES |
DIN ISO 15759:2006-05
|
Medical infusion equipment - Plastics caps with inserted elastomeric liner for containers manufactured by the blow-fill-seal (BFS) process (ISO 15759:2005) |
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 |
16/30333925 DC : 0
|
BS EN 13976-2 - RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
13/30259011 DC : 0
|
BS ISO 17218 - STERILE ACUPUNCTURE NEEDLES FOR SINGLE USE |
ISO 18746:2016
|
Traditional Chinese medicine — Sterile intradermal acupuncture needles for single 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) |
BS 7548(1992) : AMD 8538
|
SPECIFICATION FOR STERILE, SINGLE-USE SYRINGES, WITH OR WITHOUT NEEDLE, FOR INSULIN INJECTION |
BS EN ISO 8871-5:2016
|
Elastomeric parts for parenterals and for devices for pharmaceutical use Functional requirements and testing |
02/564513 DC : DRAFT OCT 2002
|
BS EN ISO 1135-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
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 |
10/30209603 DC : 0
|
BS EN ISO 11608-2 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES |
DIN 13150-1:1991-06
|
MEDICAL SYRINGES - REQUIREMENTS ON THE MEASURING SECURITY OF SYRINGS WITH SCALE - CONFORMITY TESTING AND CONFORMITY CERTIFICATION |
04/30086336 DC : 0
|
BS ISO 8871-5 - ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING |
DIN 13098-1:1992-05
|
SINGLE USE PLASTICS SYRINGES FOR MEDICAL PURPOSES - SINGLE USE PLASTICS SYRINGES FOR GENERAL USE - DIMENSIONS, REQUIREMENTS, TEST |
UNI EN ISO 8638 : 2014
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS |
I.S. EN ISO 7886-1:1998
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 1: SYRINGES FOR MANUAL USE (ISO 7886-1:2017) |
BIS IS 12227 : 2002(R2017)
|
STERILE SINGLE-USE SYRINGES, WITH OR WITHOUT NEEDLE, FOR INSULIN |
I.S. EN ISO 1135-3:2017
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
ISO/TR 19244:2014
|
Guidance on transition periods for standards developed by ISO/TC 84 — Devices for administration of medicinal products and catheters |
ISO 11070:2014
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Sterile single-use intravascular introducers, dilators and guidewires |
ISO 11040-4:2015
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Prefilled syringes Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling |
I.S. EN ISO 7886-4:2009
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STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
I.S. EN 13976-2:2011
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RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
I.S. EN ISO 8536-4:2013
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010) |
NF EN ISO 7886-3 : 2009
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STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION |
BS EN ISO 8536-4 : 2013
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
DIN EN ISO 8536-4:2013-07
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013) |
DIN EN ISO 11608-2 E : 2012
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NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 2: NEEDLES (ISO 11608-2:2012) |
BS EN ISO 11608-2:2012
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Needle-based injection systems for medical use. Requirements and test methods Needles |
UNE-EN ISO 1135-4:2016
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Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015) |
UNE-EN ISO 8537:2016
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Sterile single-use syringes, with or without needle, for insulin (ISO 8537:2016) |
BS EN ISO 7886-2:1997
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Sterile hypodermic syringes for single use Syringes for use with power-driven syringe pumps |
BS EN 13976-2:2011
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Rescue systems. Transportation of incubators System requirements |
ISO 1135-3:2016
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Transfusion equipment for medical use Part 3: Blood-taking sets for single use |
ISO 7885:2010
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Dentistry Sterile injection needles for single use |
BS EN ISO 11608-3:2012
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Needle-based injection systems for medical use. Requirements and test methods Finished containers |
UNE-EN ISO 6009:2017
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Hypodermic needles for single use - Colour coding for identification (ISO 6009:2016) |
ISO 1135-4:2015
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Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
UNE-EN ISO 22413:2013
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Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010) |
BS EN ISO 8537:2016
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Sterile single-use syringes, with or without needle, for insulin |
BS EN ISO 10555-5:2013
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Intravascular catheters. Sterile and single-use catheters Over-needle peripheral catheters |
BS EN 13718-2:2015
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Medical vehicles and their equipment. Air ambulances Operational and technical requirements for air ambulances |
DIN EN ISO 11608-2:2012-12
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Needle-based injection systems for medical use - Requirements and test methods - Part 2: Needles (ISO 11608-2:2012) |
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 8536-4:2010
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Infusion equipment for medical use Part 4: Infusion sets for single use, gravity feed |
IEC 60601-2-24:2012
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Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers |
ISO 6009:2016
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Hypodermic needles for single use Colour coding for identification |
UNE-EN ISO 11070:2015
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Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014) |
EN ISO 7886-2 : 1997
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STERILE HYPODERMIC SYRINGES FOR SINGLE USE - SYRINGES FOR USE WITH POWER-DRIVEN SYRINGE PUMPS |
ISO 8537:2016
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Sterile single-use syringes, with or without needle, for insulin |
I.S. EN 13718-2:2015
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MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES |
DIN EN 13976-2 E : 2011
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RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
ISO 11608-2:2012
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Needle-based injection systems for medical use Requirements and test methods Part 2: Needles |
ISO 11608-3:2012
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Needle-based injection systems for medical use Requirements and test methods Part 3: Finished containers |
I.S. EN 13718-2:2015+A1:2020
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MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES |
EN ISO 10555-5:2013
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Intravascular catheters - Sterile and single-use catheters - Part 5: Over-needle peripheral catheters (ISO 10555-5:2013) |
EN ISO 1135-3:2017
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Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
EN ISO 8871-5:2016
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Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016) |
EN ISO 11608-2:2012
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Needle-based injection systems for medical use - Requirements and test methods - Part 2: Needles (ISO 11608-2:2012) |
EN ISO 8537:2016
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Sterile single-use syringes, with or without needle, for insulin (ISO 8537:2016) |
EN ISO 1135-5:2015
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Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015) |
EN ISO 11608-3:2012
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Needle-based injection systems for medical use - Requirements and test methods - Part 3: Finished containers (ISO 11608-3:2012) |
EN ISO 23907:2012
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Sharps injury protection - Requirements and test methods - Sharps containers (ISO 23907:2012) |
EN ISO 6009:2016
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Hypodermic needles for single use - Colour coding for identification (ISO 6009:2016) |
EN ISO 7885:2010
|
Dentistry - Sterile injection needles for single use (ISO 7885:2010) |
BS 5724-2.124(1998) : 1998
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MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFUSION PUMPS AND CONTROLLERS |
BS EN ISO 1135-3:2017
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Transfusion equipment for medical use Blood-taking sets for single use |
BS EN 60601-2-24:2015
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Medical electrical equipment Particular requirements for the basic safety and essential performance of infusion pumps and controllers |
UNE-EN ISO 8871-5:2017
|
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016) |
DIN EN ISO 8871-5:2015-08 (Draft)
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ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
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) |
BS EN 60664-4:2006
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Insulation coordination for equipment within low-voltage systems Consideration of high-frequency voltage stress |
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
|
Transfer sets for pharmaceutical preparations. Requirements and test methods |
13/30283694 DC : 0
|
BS EN ISO 1135-5 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS |
17/30348182 DC : 0
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BS EN ISO 23907 - SHARPS INJURY PROTECTION - REQUIREMENTS AND TEST METHODS - PART 1: SINGLE-USE SHARPS CONTAINERS |
UNE-EN ISO 23907:2013
|
Sharps injury protection - Requirements and test methods - Sharps containers (ISO 23907:2012) |
ISO 17218:2014
|
Sterile acupuncture needles for single use |
NF EN ISO 7886-4 : 2009
|
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 4: SYRINGES WITH RE-USE PREVENTION FEATURE |
EN 13976-2:2011
|
Rescue systems - Transportation of incubators - Part 2: System requirements |
DIN EN 13976-2:2016-03 (Draft)
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RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
ISO 7886-1:2017
|
Sterile hypodermic syringes for single use — Part 1: Syringes for manual use |
ISO 15759:2005
|
Medical infusion equipment — Plastics caps with inserted elastomeric liner for containers manufactured by the blow-fill-seal (BFS) process |
DIN EN ISO 10555-5:2013-11
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 5: OVER-NEEDLE PERIPHERAL CATHETERS (ISO 10555-5:2013) |
UNE-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) |
ISO 22413:2010
|
Transfer sets for pharmaceutical preparations Requirements and test methods |
BS EN 28362-2:1993
|
Injection containers for injectables and accessories Closures for injection vials |
DIN EN ISO 11608-3:2013-01
|
Needle-based injection systems for medical use - Requirements and test methods - Part 3: Finished containers (ISO 11608-3:2012) |
DIN EN ISO 8871-5:2017-03
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
EN 60601-2-24:2015
|
Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers |
EN ISO 1135-4 : 2015 COR 2016
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
UNI EN ISO 22413 : 2013
|
TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS |
DIN EN 13976-2:2011-08
|
RESCUE SYSTEMS - TRANSPORTATION OF INCUBATORS - PART 2: SYSTEM REQUIREMENTS |
EN 60664-4:2006/corrigendum:2006
|
INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 4: CONSIDERATION OF HIGH-FREQUENCY VOLTAGE STRESS |
DIN ISO 11040-4:2017-07
|
PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |