NA 176

DIN Standards Committee Health Technologies

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Publications of NA 176

Number: 1,428

DIN CEN ISO/TS 7552-3 2025-03 VN Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining (ISO/TS 7552-3:2024); German version CEN ISO/TS 7552-3:2024 More  Order from DIN Media
DIN 14142 2025-03 Standard First aid material - First-aid box for fire-brigade motor cars More  Order from DIN Media
DIN EN ISO 23500-2 2025-03 Standard Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2024); German version EN ISO 23500-2:2024 More  Order from DIN Media
DIN 58953-6 2025-03 Standard Sterilization - Sterile supply - Part 6: Microbial barrier testing of packaging materials for medical devices which are to be sterilized More  Order from DIN Media
DIN EN ISO 80369-20 2025-03 Standard Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods (ISO 80369-20:2024); German version EN ISO 80369-20:2024 More  Order from DIN Media
DIN EN 13795-2 2025-03 Standard Surgical clothing and drapes - Requirements and test Methods - Part 2: Clean air suits; German version EN 13795-2:2025 More  Order from DIN Media
DIN EN 13795-1 2025-03 Standard Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns; German version EN 13795-1:2025 More  Order from DIN Media
DIN EN 14683 2025-03 Standard Medical face masks - Requirements and test methods; German version EN 14683:2025 More  Order from DIN Media
DIN EN ISO 23500-1 2025-03 Standard Preparation and quality management of fluids for haemodialysis and related therapies - Part 1: General requirements (ISO 23500-1:2024); German version EN ISO 23500-1:2024 More  Order from DIN Media
ISO 15223-1 AMD 1 2025-03 Standard Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific More  Order from DIN Media

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