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Draft technical rule [WITHDRAWN]

VDI 2083 Blatt 21:2018-08 - Draft

Cleanroom technology - Cleanliness of medical products in the manufacturing process

German title
Reinraumtechnik - Reinheit von Medizinprodukten im Herstellungsprozess
Publication date
2018-08
Original language
German
Pages
56

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Publication date
2018-08
Original language
German
Pages
56

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Short description
This standard is a pracitcal aid based on a risk-based approach to identifying critical biological, chemical or particulate contaminations and, if required, to the specification of acceptance criteria (assessment of cleanliness) and for the verification (determination of cleanliness) of medical products in the production process. This applies both to the medical products themselves and to their intermediates, supplier products, etc. This standard does not cover the initial treatment and reconditioning of medical products by the user and the assessment of biological compatibility of medical products (biocompatibility as per ISO 10993 series of standards).
Content
ICS
13.040.35
Replacement amendments

This document has been replaced by: VDI 2083 Blatt 21:2019-10 .

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