SSH EN 556-2:2005

Sterilizimi i pajisjeve mjekësore - Kërkesat për pajisjet mjekësore të shënuara "Sterile" - Pjesa 2: Kërkesat për pajisjet mjekësore të trajtuara për sterilitet

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices

Scope

This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.

NOTE For the purpose of the EU Directive(s) for medical devices (see Bibliography), designating that a medical device is 'STERILE' is only permissible when a validated sterilization process has been applied. Requirements for validation and routine control of aseptic processes are specified in prEN 13824 (in preparation).

Related directives

Directives related to this standards.