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JIS MEDICAL DEVICES IV - JIS Medical Devices IV Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES I - JIS Medical Devices I Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES II - JIS Medical Devices II Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES III - JIS Medical Devices III Handbook
January 1, 2015 - JSA
A description is not available for this item.
CSA ISO 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
January 1, 2011 - CSA

Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices. NOTE Although the scope of this International Standard...

IEEE BIO-MEDICAL - BIO-MEDICAL TELEMETRY
IEEE
A description is not available for this item.
ISO 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
October 15, 2009 - ISO

Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices. NOTE Although the scope of this International Standard...

AAMI 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
January 1, 2009 - AAMI

Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices. NOTE Although the scope of this International Standard...

FORD MACHINERY/EQUIPMENT - MACHINERY & EQUIPMENT GUIDELINES
FORD
A description is not available for this item.
NSF FOOD EQUIPMENT SET - FOOD EQUIPMENT SET
NSF
A description is not available for this item.
DSF/PREN IEC 60522-1 - Medical electrical equipment – Diagnostics X-Rays – Part 1: Determination of quality equivalent filtration and permanent filtration
DS

This International Standard applies to X-RAY TUBE ASSEMBLIES and to FILTERING MATERIAL, in medical diagnostic applications up to a HIGH VOLTAGE of 150 kV. For HIGH VOLTAGES greater than 50 kV, this standard applies to X-RAY TUBE ASSEMBLIES with tungsten or tungsten-alloy TARGETS only. NOTE 1...

ASTM F1977 - Standard Test Method for Determining Initial, Fractional, Filtration Efficiency of a Vacuum Cleaner System
March 1, 2004 - ASTM

Different sampling parameters, flow rates, and so forth, for the specific applications of the equipment and test procedure Water-filtration vacuum cleaners which do not utilize a replaceable dry media filter located between the water-based filter and cleaning air exhaust are not...

IEC 60522 - Determination of the Permanent Filtration of X-Ray Tube Assemblies
February 1, 1999 - IEC

This International Standard applies to X-RAY TUBE ASSEMBLIES for medical diagnosis and RADIOTHERAPY. Object This standard defines the concept of PERMANENT FILTRATION in X-RAY TUBE ASSEMBLIES for medical diagnosis and RADIOTHERAPY and describes a method for its determination. It...

DSF/IEC TR 60522-2 ED1 - Medical electrical equipment – Diagnostics X-Rays – Part 2: Guidance and rationale on quality equivalent filtration and permanent filtration
DS

This Technical Report provides guidance and rationale for the requirements of IEC 60522-1 and its modifications versus the second edition of IEC 60522.

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