EN 60601-2-23:1997
(Main)Medical electrical equipment - Part 2: Particular requirements for the safety of transcutaneous partial pressure monitoring equipment
Medical electrical equipment - Part 2: Particular requirements for the safety of transcutaneous partial pressure monitoring equipment
Specifies the particular requirements for the safety of transcutaneous partial pressure monitoring equipment. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.
Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von Geräten für die transkutane Partialdrucküberwachung
Appareils électromédicaux - Partie 2: Règles particulières de sécurité pour les appareils de surveillance de la pression partielle transcutanée
Spécifie les règles particulières de sécurité pour les appareils de surveillance de la pression partielle transcutanée. S'applique aux moniteurs transcutanés utilisés sur des adultes, des enfants et des nouveau-nés et inclut l'utilisation de ces dispositifs dans la surveillance foetale pendant l'accouchement.
Medical electrical equipment - Part 2: Particular requirements for the safety of transcutaneous artial pressure monitoring equipment (IEC 60601-2-23:1993)
General Information
- Status
- Withdrawn
- Publication Date
- 15-Dec-1997
- Withdrawal Date
- 31-Aug-1998
- 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-Jan-2003
- Completion Date
- 01-Jan-2003
Relations
- Effective Date
- 29-Jan-2023
Get Certified
Connect with accredited certification bodies for this standard
BSI Group
BSI (British Standards Institution) is the business standards company that helps organizations make excellence a habit.
TÜV Rheinland
TÜV Rheinland is a leading international provider of technical services.
TÜV SÜD
TÜV SÜD is a trusted partner of choice for safety, security and sustainability solutions.
Sponsored listings
Frequently Asked Questions
EN 60601-2-23:1997 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2: Particular requirements for the safety of transcutaneous partial pressure monitoring equipment". This standard covers: Specifies the particular requirements for the safety of transcutaneous partial pressure monitoring equipment. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.
Specifies the particular requirements for the safety of transcutaneous partial pressure monitoring equipment. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.
EN 60601-2-23:1997 is classified under the following ICS (International Classification for Standards) categories: 11.040.50 - Radiographic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-23:1997 has the following relationships with other standards: It is inter standard links to EN 60601-2-23:2000. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-23:1997 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 60601-2-23:1997 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)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Medical electrical equipment - Part 2: Particular requirements for the safety of transcutaneous artial pressure monitoring equipment (IEC 60601-2-23:1993)Medizinische elektrische Geräte -- Teil 2: Besondere Festlegungen für die Sicherheit von Geräten für die transkutane PartialdrucküberwachungAppareils électromédicaux -- Partie 2: Règles particulières de sécurité pour les appareils de surveillance de la pression partielle transcutanéeMedical electrical equipment -- Part 2: Particular requirements for the safety of transcutaneous partial pressure monitoring equipment11.040.50Radiografska opremaRadiographic equipmentICS:Ta slovenski standard je istoveten z:EN 60601-2-23:1997SIST EN 60601-2-23:1998en01-september-1998SIST EN 60
...
Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.
Loading comments...