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>UNE EN IEC 60601-2-34:2024 - Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment (Endorsed by Asociación Española de Normalización in February of 2025.)
sklademVydáno: 2025-02-01
UNE EN IEC 60601-2-34:2024 - Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment (Endorsed by Asociación Española de Normalización in February of 2025.)

UNE EN IEC 60601-2-34:2024

Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment (Endorsed by Asociación Española de Normalización in February of 2025.)

Equipos electromédicos. Parte 2-34: Requisitos particulares para la seguridad básica y funcionamiento esencial de equipos de vigilancia invasiva de la presión sanguínea. (Ratificada por la Asociación Española de Normalización en febrero de 2025.)

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Označení normy:UNE EN IEC 60601-2-34:2024
Počet stran:71
Vydáno:2025-02-01
Status:Norma
DESCRIPTION

UNE EN IEC 60601-2-34:2024

201.1 Scope, object and related standards Clause 1 of the general standard1 applies, except as follows: 201.1.1 *Scope Replacement: This particular standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT as defined in 201.3.63, hereinafter also referred to as ME EQUIPMENT. This document applies to INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT intended for use in professional healthcare facilities and in the EMERGENCY MEDICAL SERVICE ENVIRONMENT. This particular standard does not apply to catheter tubing, catheter needles, Luer locks, taps and tap tables that connect to the DOME. This particular standard does not apply to non-invasive blood pressure monitoring equipment. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as follows: The clause or subclause applies to ME EQUIPMENT, as default. For ME EQUIPMENT with the corresponding safety measure or function not completely integrated into the ME EQUIPMENT but instead implemented in an ME SYSTEM, the ME EQUIPMENT MANUFACTURER shall specify in the ACCOMPANYING DOCUMENTS which functionality and safety requirements shall be provided by the ME SYSTEM to comply with this standard. The ME SYSTEM has to be verified accordingly. 201.1.2 Object Replacement: The object of this particular standard is to establish BASIC SAFETY and ESSENTIAL PERFORMANCE requirements for INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT, as defined in 201.3.63.

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