EN 60601-2-23:2000
(Main)Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment
Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment
Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.
Medizinische elektrische Geräte - Teil 2-23: Besondere Festlegungen für die Sicherheit einschließlich wesentlicher Leistungsmerkmale von Geräten für die transkutane Partialdrucküberwachung
Appareils électromédicaux - Partie 2-23: Règles particulières de sécurité et performances essentielles des appareils de surveillance de la pression partielle transcutanée
Medicinska električna oprema - 2-23. del: Posebne varnostne zahteve za opremo za transkutano (skozikožno) nadzorovanje delnega tlaka (IEC 60601-2-23:1999)
General Information
- Status
- Withdrawn
- Publication Date
- 14-Mar-2000
- 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
- 15-Sep-2018
- Completion Date
- 15-Sep-2018
- Directive
- 93/42/EEC - Medical devices
Relations
- Effective Date
- 29-Jan-2023
- Effective Date
- 28-Jan-2023
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
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Frequently Asked Questions
EN 60601-2-23:2000 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment". This standard covers: Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.
Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.
EN 60601-2-23:2000 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-23:2000 has the following relationships with other standards: It is inter standard links to EN 60601-2-23:1997, EN 60601-2-23:2015, EN 60601-1-1:1993, EN 61000-4-6:1996, EN 60601-1-2:1993, EN 60601-1-4:1996, EN 60601-3-1:1996, EN 61000-4-3:1996. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-23:2000 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/432. 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 60601-2-23:2000 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)
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Medical electrical equipment - Part 2-23: Particular requirements for the safety, including
essential performance, of transcutaneous partial pressure monitoring equipment (IEC
60601-2-23:1999)
Medizinische elektrische Geräte - Teil 2-23: Besondere Festlegungen für die Sicherheit
einschließlich wesentlicher Leistungsmerkmale
...
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