ISO 17664

Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices

2004-03-00

Có hiệu lực

DIN EN ISO 17664 (2004-07), IDT * BS EN ISO 17664 (2004-03-12), IDT * EN ISO 17664 (2004-03), IDT * NF S98-116 (2004-08-01), IDT * CAN/CSA-Z17664-06 (2006-04-01), IDT * SN EN ISO 17664 (2004-05), IDT * OENORM EN ISO 17664 (2004-06-01), IDT * PN-EN ISO 17664 (2005-12-08), IDT * SS-EN ISO 17664 (2004-10-08), IDT * UNE-EN ISO 17664 (2004-09-30), IDT * GOST R ISO 16061 (2011), IDT * GOST R ISO 17664 (2012), IDT * UNI EN ISO 17664:2005 (2005-06-01), IDT * STN EN ISO 17664 (2004-09-01), IDT * CSN EN ISO 17664 (2004-11-01), IDT * DS/EN ISO 17664 (2004-04-13), IDT * NEN-EN-ISO 17664:2004 en (2004-04-01), IDT * SANS 17664:2007 (2007-11-28), IDT

ISO/FDIS 17664 (2003-07)

ISO 17664 (2004-03) * ISO/FDIS 17664 (2003-07) * ISO/DIS 17664 (2001-04)

Capability of sterilization * Characterisations * Cleaning * Consumer-supplier relations * Data of the manufacturer * Decontaminations * Definitions * Disinfection * Enterprises * Health protection * Hygiene * Instructions * Medical devices * Medical equipment * Medical products * Packages * Product information * Reprocessing * Reuse * Risk analysis * Sequence of operations * Specification * Specification (approval) * Sterilization (birth control) * Sterilization (hygiene) * Sterilized goods * Sterilizers * Surveillance (approval) * Treatment * Validation * Verification * Purification * Preparation

11.080.01. Thanh trùng và khử trùng nói chung

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