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SK EN ISO 14160:2011

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SK EN ISO 14160:2011
Status: Withdrawn
Gjuha: English
Faqe: 23
Publikuar: 2011-08-01
I tërhequr: 2024-02-27
Regjistri Kombëtar: 80/2011
Botim:
Standardet ndërkombëtare që kanë lidhje
This standard is identical to:
EN ISO 14160:2011
CEN/TC 204
Çmim: 25 €



Titulli Shqip

Sterilizimi i pajisjeve mjekësore me një përdorim të fiksuara ne materialet me origjinë shtazore -Jetëgjatësia dhe kontrolli rutinë i sterilizimit me anë te solucioneve kimike sterilizuese

Titulli Anglisht

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 (ISO 14160:2011)

Scope Shqip

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Scope Anglisht

ISO 14160:2011 specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid chemical sterilizing agents of single-use medical devices comprising, in whole or in part, materials of animal origin. ISO 14160:2011 covers the control of risks arising from contamination with bacteria and fungi by application of a liquid chemical sterilization process. Risks associated with other microorganisms need to be assessed. ISO 14160:2011 is not applicable to material of human origin. ISO 14160:2011 does not describe methods for the validation of the inactivation of viruses and transmissible spongiform encephalopath (TSE) agents. ISO 14160:2011 does not describe methods for validation of the inactivation, elimination, or elimination and inactivation of protozoa and parasites. The requirements for validation and routine control described in ISO 14160:2011 are only applicable to the defined sterilization process of a medical device, which is performed after the manufacturing process, and do not take account of the lethal effects of other bioburden reduction steps. ISO 14160:2011 does not specify tests to establish the effects of any chosen sterilization method upon the fitness for use of the medical device. ISO 14160:2011 does not cover the level of residual sterilizing agent within medical devices. ISO 14160:2011 does not describe a quality management system for the control of all stages of manufacture.

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