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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.30 Surgical instruments and materials>BS EN IEC 60601-2-2:2018 Medical electrical equipment Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories
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immediate downloadReleased: 2018-06-05
BS EN IEC 60601-2-2:2018 Medical electrical equipment Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories

BS EN IEC 60601-2-2:2018

Medical electrical equipment Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories

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Standard number:BS EN IEC 60601-2-2:2018
Pages:96
Released:2018-06-05
ISBN:978 0 580 89316 2
Status:Standard
DESCRIPTION

BS EN IEC 60601-2-2:2018


This standard BS EN IEC 60601-2-2:2018 Medical electrical equipment is classified in these ICS categories:
  • 11.040.30 Surgical instruments and materials
IEC 60601-2-2:2017 is also available as IEC 60601-2-2:2017 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 60601-2-2:2017 applies to the basic safety and essential performance of HF surgical equipment and HF surgical accessories.
HF surgical equipment having a rated output power not exceeding 50 W (for example for micro-coagulation, or for use in dentistry or ophthalmology) is exempt from certain of the requirements of this particular standard. These exemptions are indicated in the relevant requirements.
The object of this particular standard is to establish particular basic safety and essential performance requirements for HF surgical equipment and HF surgical accessories. This sixth edition cancels and replaces the fifth edition published in 2009. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
- refinement and additions to the defined terms;
- additional separation of the requirements for HF surgical equipment and HF surgical accessories;
- a new requirement for adult neutral electrodes to be contact quality monitoring neutral electrodes;
- new requirements for devices that have or use a high current mode.