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DIN EN ISO 10993-4:2025-09

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood.
(Biologische Beurteilung von Medizinprodukten - Teil 4: Auswahl von Prüfungen zur Wechselwirkung mit Blut.)

Standard published on 1.9.2025

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287.00 USD


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DIN EN ISO 10993-5:2009-10

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.
(Biologische Beurteilung von Medizinprodukten - Teil 5: Prüfungen auf In-vitro-Zytotoxizität.)

Standard published on 1.10.2009

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179.20 USD


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DIN EN ISO 10993-5/A11:2025-05 Change

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.
(Biologische Beurteilung von Medizinprodukten - Teil 5: Prüfungen auf In-vitro-Zytotoxizität.)

Change published on 1.5.2025

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82.20 USD


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DIN EN ISO 10993-6:2017-09

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation.
(Biologische Beurteilung von Medizinprodukten - Teil 6: Prüfungen auf lokale Effekte nach Implantationen.)

Standard published on 1.9.2017

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179.20 USD


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E DIN EN ISO 10993-6:2024-06

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation.
(Biologische Beurteilung von Medizinprodukten - Teil 6: Prüfungen auf lokale Effekte nach Implantationen.)

Standard published on 1.6.2024

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164.20 USD


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DIN EN ISO 10993-7:2022-09

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals.
(Biologische Beurteilung von Medizinprodukten - Teil 7: Ethylenoxid-Sterilisationsrückstände.)

Standard published on 1.9.2022

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287.00 USD


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E DIN EN ISO 10993-7:2024-08

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals.
(Biologische Beurteilung von Medizinprodukten - Teil 7: Ethylenoxid-Sterilisationsrückstände.)

Standard published on 1.8.2024

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291.10 USD


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DIN EN ISO 10993-9:2022-03

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products.
(Biologische Beurteilung von Medizinprodukten - Teil 9: Rahmen zur Identifizierung und Quantifizierung von möglichen Abbauprodukten.)

Standard published on 1.3.2022

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123.70 USD


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VDA 11

Ermittlung des Reifenrobustheits-Faktors - Arbeitsanweisung für neue PKW-Reifen mit Notlaufeigenschaften / Calculation of Tire-Robustness-Factor - VDA Test Procedure for new Passenger car-tires with Runflat performance (Version 04/2016) - Gruppenlizenz (group license), AGB (GTC) Art. 10, 2

Standard published on 1.4.2016

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German -
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VDA 11-007

Vorlage zur Erstellung eines Sicherheitsdatenblatts für pyrotechnische Gegenstände für Fahrzeuge gemäß Artikel 11 Abs. 3 der Richtlinie 2013/29/EU in Verbindung mit Verordnung (EG) Nr. 1907/2006 (REACH), Anhang II 07/2024) - Gruppenlizenz (group license), AGB (GTC) Art. 10, 2 - Language of the document German

Standard published on 1.7.2024

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ON REQUEST


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