Cover E DIN EN 60601-2-68/A1 VDE 0750-2-68/A1:2021-03
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E DIN EN 60601-2-68/A1 VDE 0750-2-68/A1:2021-03

Electrical medical equipment

Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment

(IEC 62C/774/CD:2020); Text in German and English
Class/Status: Draft, valid
Released: 2021 -03   Published: 2021-02 -26
VDE Art. No.: 1701601
End of objection deadline: 2021-04-26

This draft amendment deals with safety aspects of Megavolt-MV-) systems for imaging related to external beam system, electron accelerator, light ion- beam therapy system and radionuclid- beam therapy system.
Since the edition 1 was published changes took place in the standards environment.
The following standards relevant to x-igrt equipment were updated, or newly published:
– IEC 60601-2-1:2020, Requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV
– IEC 60601-2-64, Requirements for the basic safety and essential performance of light ion beam medical electrical equipment
– IEC TR 62926 has been modified during it’s development and was not published as an international standard but as a technical report and provides guidance for integration of electron accelerators with other equipment.
– IEC TR 63183 provides guidance on the construction of error and warning messages.
This amendment extends the scope of IEC 60601-2-68 to ct scanners, intended to be used in the same room with an external beam equipment.

Title Format
Entwicklung und Herstellung medizinischer Software
Prinz, Thorsten (Hrsg.)

Entwicklung und Herstellung medizinischer Software

Normen in der Medizintechnik
VDE-Schriftenreihe – Normen verständlich, Band 171

2017, 219 pages, Din A5, Broschur

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