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Standards [CURRENT]

DIN EN ISO 10993-16

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017); German version EN ISO 10993-16:2017
Edition 2018-02

Standards [CURRENT]

DIN ISO 22935-2

Milk and milk products - Sensory analysis - Part 2: Recommended methods for sensory evaluation (ISO 22935-2:2009)
Edition 2012-12

Standards [CURRENT]

DIN EN 12353

Chemical disinfectants and antiseptics - Preservation of test organisms used for the determination of bactericidal (including Legionella), mycobactericidal, sporicidal, fungicidal and virucidal (including bacteriophages) activity; German version EN 12353:2021
Edition 2021-11

Standards [CURRENT]

DIN EN ISO 11979-6

Ophthalmic implants - Intraocular lenses - Part 6: Shelf-life and transport stability testing (ISO 11979-6:2014); German version EN ISO 11979-6:2014
Edition 2015-02

Standards [CURRENT]

DIN EN ISO 6710

Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017
Edition 2017-12

Standards [CURRENT]

DIN EN 15652

Foodstuffs - Determination of niacin by HPLC; German version EN 15652:2009
Edition 2009-09

Standards [available pre-publication]

DIN EN ISO 18113-2

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022); German version EN ISO 18113-2:2024
Edition 2024-10

Standards [CURRENT]

DIN EN ISO 22442-2

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020); German version EN ISO 22442-2:2020
Edition 2021-04

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 18113-2

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/DIS 18113-2:2021); German and English version prEN ISO 18113-2:2021
Edition 2021-09

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