Need help?

EN 62220-1-2:2007 Standard

wave
Save  

  Keywords:

#digital #systems #part #imaging #ray

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Friday 17th of November 2017

  Description:

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

  Purpose

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).

  Publication

Friday 17th of November 2017

  Related Standards

EN 60627:2001

Medical devices Directive (93/42/EEC)

Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter gridsIEC 60627:2001

EN 1789:2007 +A1:2010

Medical devices Directive (93/42/EEC)

Medical vehicles and their equipment - Road ambulances

EN 556-1:2001

Medical devices Directive (93/42/EEC)

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminal...

EN 556-1:2001/AC:2006

Medical devices Directive (93/42/EEC)

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminal...

EN 556-2:2015

Medical devices Directive (93/42/EEC)

Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptic...

EN 794-3:1998 +A2:2009

Medical devices Directive (93/42/EEC)

Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators

  Stay up to date

CELAB is Notified Body No.2037 for the EMC Directive and Italian office of a Notified Body for the RED Directive.

CELAB performs voluntary inspection activities on technical construction files to check their contents.

CELAB can accomplish all the required tests in order to affix the CE-marking related to EMC, LVD, RED, MDD, machines and many others.

CLICK HERE TO GET TESTS AND INFO ON THE EN 62220-1-2:2007 STANDARD

  ACCESS

Search for a standard
GO

Register

Already a member?
Login

  OTHER APPLICATIONS

If you are interested in DO160 tests, you can give a try to our other free of charge software:
CE-Marking assistant, Version: 1.3.0