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CSA Z314.3

6th Edition, January 1, 2014

Complete Document

Effective sterilization in health care settings by the steam process

Includes all amendments and changes through Errata , January 2015


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Superseded By: CSA Z314

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Additional Comments:
W/D S/S BY CSA Z314
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Product Details:

  • Revision: 6th Edition, January 1, 2014
  • Published Date: January 2015
  • Status: Superseded By:
  • Superseded By: CSA Z314
  • Document Language: English
  • Published By: CSA Group (CSA)
  • Page Count: 91
  • ANSI Approved: No
  • DoD Adopted: No

Description / Abstract:

This Standard specifies essential elements for using steam to sterilize medical devices in health care settings, with the object of achieving an adequate level of sterility assurance and minimizing the risk of injury to health care setting personnel and patients. Notes:

1) The term "health care setting" includes, but is not limited to, hospitals, nursing homes, extended-care facilities, clinics, medical and dental offices, and health units in industry. See CSA Z314.0 for a more comprehensive definition.

2) Comprehensive guidance for small, community health care settings can be found in CSA SPE-1112.

This Standard includes requirements for

a) sterilization equipment including tabletop sterilizers;

b) preparation and packaging of medical devices requiring sterilization;

c) sterilizer loading and operation;

d) sterility assurance, including process challenge device (PCD) construction and use; and

e) immediate use steam sterilization (IUSS).

Note: IUSS (also known as flash or emergency sterilization) is usually performed outside of the MDRD.

This Standard does not apply to

a) manufacturers' requirements for construction and performance of steam sterilizers;

Note: See CAN/CSA-Z314.7.

b) washer/sterilizers;

c) decontamination of reusable medical devices prior to sterilization;

Note: See CSA Z314.8.

d) chemical sterilization;

Note: See CSA Z314.23.

e) single-use/disposable medical devices; or

Note: See the Canadian Healthcare Association, the ECRI Institute, and the Canadian Agency for Drugs and Technologies in Health.

f) medical devices that have been used with patients who are known or suspected to haveCreutzfeldt-Jakob Disease (CJD) or prion-related diseases.

Note: See Public Health Agency of CanadaClassic Creutzfeldt-Jakob Disease in Canada — Quick Reference Guide and Classic Creutzfeldt-Jakob Disease in Canada.

In this Standard, "shall" is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the standard; "should" is used to express a recommendation or that which is advised but not required; and "may" is used to express an option or that which is permissible within the limits of the standard.

Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material.

Notes to tables and figures are considered part of the table or figure and may be written as requirements.

Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.
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