Committee
|
CTN 111 |
Document Type
|
Standard |
ISBN
|
|
Pages
|
|
Published
|
|
Publisher
|
Asociacion Espanola de Normalizacion
|
Status
|
Current |
Supersedes
|
|
ISO 3826-2:2008
|
Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets |
ISO 10993-4:2017
|
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 |
ISO 3826-1:2013
|
Plastics collapsible containers for human blood and blood components Part 1: Conventional containers |
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 |
ISO 3696:1987
|
Water for analytical laboratory use — Specification and test methods |
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols |
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 |
ISO 594-1:1986
|
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements |
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 |
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