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Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)

99.60 Withdrawal effective

CEN/TC 206

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)

99.60 Withdrawal effective

CEN/TC 206

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)

99.60 Withdrawal effective

CEN/TC 206

Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000)

99.60 Withdrawal effective

CEN/TC 206

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013)

99.60 Withdrawal effective

CEN/TC 204

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006)

99.60 Withdrawal effective

CEN/TC 204

Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012)

99.60 Withdrawal effective

CEN/TC 204

Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)

99.60 Withdrawal effective

CEN/TC 204

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006/Amd 1:2014)

99.60 Withdrawal effective

CEN/TC 102

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/Amd 1:2014)

99.60 Withdrawal effective

CEN/TC 102

Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)

99.60 Withdrawal effective

CEN/TC 204

Non-active surgical implants - Body contouring implants - Specific requirements for mammary implants

99.60 Withdrawal effective

CEN/TC 285

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures

99.60 Withdrawal effective

CEN/TC 140

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures

99.60 Withdrawal effective

CEN/TC 140

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials

99.60 Withdrawal effective

CEN/TC 140

Breathing system filters for anaesthetic and respiratory use - Part 1: Salt test method to assess filtration performance

99.60 Withdrawal effective

CEN/TC 215

Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)

99.60 Withdrawal effective

CEN/TC 204

Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)

99.60 Withdrawal effective

CEN/TC 204