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DIN EN ISO 17351
Packaging - Braille on packaging for medicinal products (ISO 17351:2013); German version EN ISO 17351:2014
Edition
2014-10
DIN EN 14885
Chemical disinfectants and antiseptics - Application of European Standards for chemical disinfectants and antiseptics; German version EN 14885:2022 + AC:2023
Edition
2023-07
DIN ISO 13022
Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
Edition
2014-06
DIN EN 868-8
Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods; German version EN 868-8:2018
Edition
2019-03
DIN EN ISO 14630
Non-active surgical implants - General requirements (ISO 14630:2012); German version EN ISO 14630:2012
Edition
2013-03
DIN EN ISO 11240
Health informatics - Identification of medicinal products - Data elements and structures for unique identification and exchange of units of measurement (ISO 11240:2012); German version EN ISO 11240:2012
Edition
2013-03
DIN EN 868-4
Packaging for terminally sterilized medical devices - Part 4: Paper bags - Requirements and test methods; German and English version prEN 868-4:2024
Edition
2024-05
DIN EN ISO 27953-2
Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: Human pharmaceutical reporting requirements for ICSR (ISO 27953-2:2011); German and English version EN ISO 27953-2:2011, only on CD-ROM
Edition
2012-09
DIN EN ISO 18362
Manufacture of cell-based health care products - Control of microbial risks during processing (ISO 18362:2016); German and English version prEN ISO 18362:2018
Edition
2018-11
DIN EN 868-5
Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods; German version EN 868-5:2018
Edition
2019-03