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Standards [CURRENT]

DIN EN ISO 11239

Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (ISO 11239:2023); German version EN ISO 11239:2023
Edition 2023-10

Standards [Pre-order]

DIN EN ISO 5361

Anaesthetic and respiratory equipment - Tracheal tubes and connectors (ISO 5361:2023); German version EN ISO 5361:2023
Edition 2023-08

Standards [CURRENT]

DIN EN ISO 21649

Needle-free injection systems for medical use - Requirements and test methods (ISO 21649:2023); German version EN ISO 21649:2023
Edition 2023-06

Draft standard

DIN EN ISO 80369-6

Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neural applications (ISO/DIS 80369-6:2023); German and English version prEN ISO 80369-6:2023
Edition 2023-09

Standards [CURRENT]

DIN EN ISO 80369-20

Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods (ISO 80369-20:2015); German version EN ISO 80369-20:2015
Edition 2015-09

Standards [CURRENT]

DIN EN ISO 18113-3

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011
Edition 2013-01

Draft standard

DIN EN ISO 7197

Neurosurgical implants - Sterile, single-use hydrocephalus shunts (ISO/DIS 7197:2023); German and English version prEN ISO 7197:2023
Edition 2023-07

Standards [CURRENT]

DIN EN 13976-2

Rescue systems - Transportation of incubators - Part 2: System requirements; German version EN 13976-2:2018
Edition 2018-09

Standards [CURRENT]

DIN EN ISO 18777

Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005); German version EN ISO 18777:2009
Edition 2009-07

Standards [available pre-publication]

DIN EN ISO 18113-1

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022); German version EN ISO 18113-1:2024
Edition 2024-10

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