DIN/TS 5343:2022 Edition
$24.70
Cleanliness of medical devices – Risk orientated validation of cleanliness, development of acceptance criteria and selection of test methods
Published By | Publication Date | Number of Pages |
DIN | 2022-04 | 39 |
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This document specifies requirements to ensure the required cleanliness of medical devices in their delivery state. In addition, this document specifies requirements to ensure the cleanliness of medical devices required for further steps in the manufacturing process which are necessary to produce a safe medical device. Processes which are carried out after opening the original packaging of the medical device are not covered by this document.
Published Code | DIN |
---|---|
Published By | Deutsches Institut für Normung |
Publication Date | 2022-04 |
Pages Count | 39 |
Language | Germany |
Descriptors | Acceptance, Acceptance (approval), Acceptance control, Cleaning, Contamination, Definitions, Examination (quality assurance), Hygiene, Impurities, Inspection, Medical devices, Medical products, Medical sciences, Methods of manufacture, Monitoring, Process, Process monitoring, Production, Purity, Quality management, Risk, Risk analysis, Specification (approval), Testing, Reception |
File Size | 2.3 MB |
ICS Codes | 11.040.01 - Medical equipment in general |
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