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SRPS IEC 60601-2-2:1999

Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment

Jan 27, 1999
Jan 27, 1999
95.99   Withdrawal of Standard   Mar 31, 2011

General information

95.99     Mar 31, 2011

ISS

N062

European Norm

Serbian  

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Scope

This clause of the General Standard applies except as follows: Addition: This Particular Standard specifies requirements for the safety of HIGH FREQUENCY SURGICAL EQUIPMENT used in medical practice, as defined in 2.1.101, hereinafter referred to as EQUIPMENT. EQUIPMENT having a rated output power not exceeding 50 W (for example for micro-coagulation, or for use in dentistry or ophthalmology) is exempted from certain of the requirements of this Standard. These exemptions are indicated in the relevant requirements.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS N.S5.605:1985

NOW

WITHDRAWN
SRPS IEC 60601-2-2:1999
95.99 Withdrawal of Standard
Mar 31, 2011

REVISED BY

WITHDRAWN
SRPS EN 60601-2-2:2011

Related project

Adopted from EN 60601-2-2:1993