IEC 60601-2-65:2012/AMD2:2021

Amendment 2 - Medical electrical equipment - Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment

IEC 60601-2-65:2012/AMD2:2021

Name:IEC 60601-2-65:2012/AMD2:2021   Standard name:Amendment 2 - Medical electrical equipment - Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment
Standard number:IEC 60601-2-65:2012/AMD2:2021   language:English language
Release Date:02-May-2021   technical committee:SC 62B - Medical imaging equipment, software, and systems
Drafting committee:WG 39 - TC 62/SC 62B/WG 39   ICS number:11.040.50 - Radiographic equipment

IEC 60601-2-65
Edition 1.0 2021-05
INTERNATIONAL
STANDARD
AMENDMENT 2
Medical electrical equipment –
Part 2-65: Particular requirements for the basic safety and essential performance
of dental intra-oral X-ray equipment

IEC 60601-2-65:2012-09/AMD2:2021-05(en)





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IEC 60601-2-65
Edition 1.0 2021-05
INTERNATIONAL
STANDARD
AMENDMENT 2
Medical electrical equipment –

Part 2-65: Particular requirements for the basic safety and essential

performance of dental intra-oral X-ray equipment

INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
ICS 11.040.50 ISBN 978-2-8322-9630-1

– 2 – IEC 60601-2-65:2012/AMD2:2021
© IEC 2021
FOREWORD
This second amendment has been prepared by subcommittee 62B: Diagnostic imaging
equipment, of IEC technical committee 62: Electrical equipment in medical practice.
The text of this amendment is based on the following documents:
FDIS Report on voting
62B/1233/FDIS 62B/1238/RVD
Full information on the voting for the approval of this amendment can be found in the report on
voting indicated in the above table.
The committee has decided that the contents of this amendment and the base publication will
remain unchanged until the stability date indicated on the IEC website under
"http://webstore.iec.ch" in the data related to the specific publication. At this date, the
publication will be
• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
_____________
201.7.9.1 General
Add, under Addition, after the existing second paragraph, the following new text and new note:
QUALITY CONTROL PROCEDURE recommended by the MANUFACTURER requires a
If a test or a
device-specific arrangement (including a tool, a phantom, a special software or a software
setting); that is only available from the MANUFACTURER, the MANUFACTURER shall provide this
arrangement for the RESPONSIBLE ORGANIZATION.
NOTE 102 The intention is to perform these QUALITY CONTROL PROCEDURES and tests using only the supplied
information.
203.5.2.4.5 Deterministic effects
Add, after the note of this subclause, the following new subclause:
203.5.2.4.6 RISK to OPERATORS
Addition:
NOTE OPERATORS of HAND-HELD ME EQUIPMENT are assumed to be in the SIGNIFICANT ZONE OF OCCUPANCY when the
ME equipment is hand-held during LOADING.
203.6.2.1 Normal initiati
...

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