Standard Swedish standard · SS-EN 556-2:2015

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

Status: Valid

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 permissible when a validated manufacturing and sterilization process has been applied. Requirements for validation and routine control of aseptic processes are specified in EN ISO 13408 1. Specific requirements for the aseptic processing of solid medical devices and combination products are specified in ISO 13408 7.

Subjects

Sterilization and disinfection in general (11.080.01)


Product information

Language: English

Written by: SIS - Standardiseringens stöd

International title:

Article no: STD-8015813

Edition: 2

Approved: 9/9/2015

No of pages: 28

Replaces: SS-EN 556-2:2004