BS EN 556-2. Sterilization of medical devices. Requirements for medical devices to be designated ''STERILE" Part 2. requirements for aseptically processed medical devices
CURRENCY
Standard number:
23/30457240 DC
Pages:
20
Released:
2023-01-24
Status:
Draft for Comment
DESCRIPTION
23/30457240 DC
This standard 23/30457240 DC BS EN 556-2. Sterilization of medical devices. Requirements for medical devices to be designated ''STERILE" is classified in these ICS categories:
11.080.01 Sterilization and disinfection in general
11.080.01 Sterilization and disinfection in general
This document 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.
