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BSI BS EN 13824:2004

Sterilization of medical devices. Aseptic processing of liquid medical devices. Requirements

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BSI BS EN 13824:2004

Sterilization of medical devices. Aseptic processing of liquid medical devices. Requirements

PUBLISH DATE 2004

PAGES 64

Document Information

Sterilization of medical devices. Aseptic processing of liqu


SDO	BSI: British Standards Institution
Document Number	EN 13824
Publication Date	Dec. 6, 2004
Language	en - English
Page Count	64
Revision Level
Supercedes
Committee	CH/198

Publish Date	Document Id	Type	View
Dec. 6, 2004	BS EN 13824:2004	Revision

SDO	Document	Title
BSI	BSI BS EN 556-2	Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE' -- Requirements for aseptically processed medical devices
BSI	BSI BS EN 556-1	Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE' -- Requirements for terminally sterilized medical devices
AAMI	AAMI TIR28	Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE'
ISO	ISO 14160	Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
BSI	BSI BS EN ISO 14160	Sterilization of health care products. Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives. Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
BSI	BSI BS EN 556	Sterilization of medical devices. Requirements for terminally-sterilized devices to be labelled 'Sterile'
BSI	BSI BS EN 15424	Sterilization of medical devices. Low temperature steam and formaldehyde. Requirements for development, validation and routine control of a sterilization process for medical devices
BSI	BSI BS EN ISO 17664-2	Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices -- Non-critical medical devices
BSI	BSI BS EN 868-6	Packaging for terminally sterilized medical devices -- Paper for low temperature sterilization processes. Requirements and test methods
AAMI	ANSI/AAMI/ISO 17664-2	Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 2: Non-critical medical devices
CSA	CSA ISO 17664-2	Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices (Adopted ISO 17664-2:2021, first edition, 2021-02)
ISO	ISO 17664-2	Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices
BSI	BSI BS EN ISO 17664-1	Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices -- Critical and semi-critical medical devices
ISO	ISO 17664-1	Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices
CSA	CSA ISO 17664-1	Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices (Adopted ISO 17664-1:2021, first edition, 2021-07)
AAMI	ANSI/AAMI/ISO 17664-1	Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 1: Critical and semi-critical medical devices
ISO	ISO/TS 21387	Sterilization of medical devices - Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
BSI	BSI PD ISO/TS 21387	Sterilization of medical devices. Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
BSI	BSI BS EN 868-7	Packaging for terminally sterilized medical devices -- Adhesive coated paper for low temperature sterilization processes. Requirements and test methods
BSI	BSI PD IEC/TR 80002-3	Medical device software -- Process reference model of medical device software life cycle processes (IEC 62304)
BSI	BSI PD ISO/TS 22421	Sterilization of health care products. Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
ISO	ISO/TS 22421	Sterilization of health care products - Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
BSI	BSI BS EN 868-2	Packaging for terminally sterilized medical devices -- Sterilization wrap. Requirements and test methods
BSI	BSI BS EN ISO 11607-1	Packaging for terminally sterilized medical devices -- Requirements for materials, sterile barrier systems and packaging systems
AAMI	AAMI/IEC TIR80002-3	Medical Device Software—Part 3: Process reference model of medical device software life cycle processes (IEC 62304)

BSI BS EN 13824:2004

Sterilization of medical devices. Aseptic processing of liquid medical devices. Requirements

BSI BS EN 13824:2004

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