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ISO 3826-2:2008
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Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets |
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ISO 10993-4:2017
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Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
|
ISO 11135:2014
|
Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices |
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ISO 9626:2016
|
Stainless steel needle tubing for the manufacture of medical devices — Requirements and test methods |
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DIN 13097-4:2009-08
|
HYPODERMIC NEEDLES - PART 4: POINT GEOMETRY, REQUIREMENTS AND TESTING |
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DIN EN ISO 8536-14:2015-08 (Draft)
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 14: CLAMPS AND FLOW REGULATORS FOR TRANSFUSION AND INFUSION EQUIPMENT WITHOUT FLUID CONTACT (ISO 8536-14:2016) |
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DIN EN ISO 10993-4:2009-10
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 4: SELECTION OF TESTS FOR INTERACTIONS WITH BLOOD (ISO 10993-4:2017) |
|
ISO 1773:1997
|
Laboratory glassware Narrow-necked boiling flasks |
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DIN EN 80416-1:2009-11
|
BASIC PRINCIPLES FOR GRAPHICAL SYMBOLS FOR USE ON EQUIPMENT - PART 1: CREATION OF GRAPHICAL SYMBOLS FOR REGISTRATION |
|
EN ISO 7864:2016
|
Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016) |
|
DIN EN ISO 9626 E : 2016
|
STAINLESS STEEL NEEDLE TUBING FOR THE MANUFACTURE OF MEDICAL DEVICES - REQUIREMENTS AND TEST METHODS (ISO 9626:2016) |
|
ISO 7864:2016
|
Sterile hypodermic needles for single use — Requirements and test methods |
|
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
|
ISO 291:2008
|
Plastics Standard atmospheres for conditioning and testing |
|
IEC 80416-1:2008
|
Basic principles for graphical symbols for use on equipment - Part 1: Creation of graphical symbols for registration |
|
ISO 14644-1:2015
|
Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
|
DIN EN ISO 3826-2:2008-11
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 2: GRAPHICAL SYMBOLS FOR USE ON LABELS AND INSTRUCTION LEAFLETS |
|
ISO 3696:1987
|
Water for analytical laboratory use — Specification and test methods |
|
EN ISO 3696:1995
|
Water for analytical laboratory use - Specification and test methods (ISO 3696:1987) |
|
DIN 13097-5:2008-11
|
HYPODERMIC NEEDLES - PART 5: SOCKETS, HUBS AND CONNECTIONS - REQUIREMENTS AND TESTING |
|
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols |
|
ISO 11607-1:2006
|
Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
|
ISO 8536-14:2016
|
Infusion equipment for medical use Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact |
|
ISO 594-2:1998
|
Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 2: Lock fittings |
|
ISO 15223-1:2016
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
|
DIN EN ISO 291:2008-08
|
PLASTICS - STANDARD ATMOSPHERES FOR CONDITIONING AND TESTING |
|
ISO 594-1:1986
|
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements |
|
EN ISO 14644-1:2015
|
Cleanrooms and associated controlled environments - Part 1: Classification of air cleanliness by particle concentration (ISO 14644-1:2015) |
|
DIN ISO 3696:1991-06
|
WATER FOR ANALYTICAL LABORATORY USE - SPECIFICATION AND TEST METHODS |
|
ISO 17665-1:2006
|
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |