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NEN-EN 556-2

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

active, Most Current
Organization: NEN
Publication Date: 1 September 2015
Status: active
Page Count: 19
ICS Code (Sterilization and disinfection in general): 11.080.01
scope:

NEN-EN 556-2 specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.

Document History

NEN-EN 556-2
September 1, 2015
Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
NEN-EN 556-2 specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.
January 1, 2014
Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2: Requirements for aseptically processed medical devices
NEN-EN 556-2 specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.
January 1, 2004
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.
January 1, 2002
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'.

References

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