EN 60601-2-2:1993
(Main)Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment
Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment
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.
Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von Hochfrequenz-Chirurgiegeräten
Appareils électromédicaux - Partie 2: Règles particulières de sécurité pour appareils d'électrochirurgie à courant haute fréquence
Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment (IEC 601-2-2:1991)
General Information
- Status
- Withdrawn
- Publication Date
- 21-Apr-1993
- Withdrawal Date
- 14-Sep-1993
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62D - IEC_SC_62D
- Parallel Committee
- IEC/SC 62D - IEC_SC_62D
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 01-Aug-2003
- Completion Date
- 01-Aug-2003
Relations
- Effective Date
- 28-Jan-2023
Frequently Asked Questions
EN 60601-2-2:1993 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment". This standard covers: 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.
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.
EN 60601-2-2:1993 has the following relationships with other standards: It is inter standard links to EN 60601-2-2:2000. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-2:1993 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
EN 60601-2-2:1993 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
SLOVENSKI STANDARD
01-maj-1995
Medical electrical equipment - Part 2: Particular requirements for the safety of high
frequency surgical equipment (IEC 601-2-2:1991)
Medical electrical equipment -- Part 2: Particular requirements for the safety of high
frequency surgical equipment
Medizinische elektrische Geräte -- Teil 2: Besondere Festlegungen für die Sicherheit von
Hochfrequenz-Chirurgiegeräten
Appareils électromédicaux -- Partie 2: Règles particulières de sécurité pour appareils
d'électrochirurgie à courant haute fréquence
Ta slovenski standard je istoveten z: EN 60601-2-2:1993
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
S
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