IEC 62220-1-2 Edition 1.0 2007-06

Standard Organization:

IEC 62220-1-2 Edition 1.0 2007-06
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum efficiency - Detectors used in mammography

Recognition Date2010-10-04
Recognition List025
Recognition Number12-213
Extent Complete standard
Standards Orgs IEC International Electrotechnical Commission http://www.iec.ch/
STG Radiology
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Rationale:

This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.

Scope:

This part of IEC 62220 specifies the method for the determination of the DETECTIVE QUANTUM EFFICIENCY (DQE) of DIGITAL X-RAY IMAGING DEVICES as a function of AIR KERMA and of SPATIAL FREQUENCY for the working conditions in the range of the medical application as specified by the MANUFACTURER. The intended users of this part of IEC 62220 are manufacturers and well equipped test laboratories.

This Part 1-2 is restricted to DIGITAL X-RAY IMAGING DEVICES that are used for mammographic imaging such as but not exclusively, CR systems, direct and indirect flat panel detector based systems, scanning systems (CCD based or photon-counting). This part of IEC 62220 is not applicable to

- DIGITAL X-RAY IMAGING DEVICES intended to be used in general radiography or in dental radiography;

- computed tomography;

and

- devices for dynamic imaging (where series of images are acquired, as in fluoroscopic or cardiac imaging).

Code of Federal Regulations:

Regulation Number Device Name Device Class Product Code
§892.1715 Full Field Digital, System, X-Ray, Mammographic Class 2 MUE

FDA Guidance:

Draft Guidance of Industry and FDA Staff: Class II Special Controls Guidance Document: Full Field Digital Mammography System, May 30, 2008


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