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STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 2: REQUIREMENTS FOR ASEPTICALLY PROCESSED MEDICAL DEVICES
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Published date: 12-01-2013
Publisher: Netherlands Standards
ForewordIntroduction1 Scope2 Normative references3 Terms and definitions4 RequirementsAnnex ZA (informative) Clauses of this European Standard addressing essential requirements or other provisions of EU DirectivesBibliography
Defines the requirements for an aseptically processed medical device to be designated 'STERILE'.
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