Norm

NEN-EN-ISO 80601-2-61:2009 Ontw. en

Medische elektrische toestellen - Speciale eisen voor basisveiligheid en essentiĆ«le prestaties van pulse oximeterapparatuur voor medisch gebruik - Deel 2-61

  • Deze norm is ingetrokken sinds 15-04-2011

47,60 57,60 Incl BTW

Over deze norm

Status Ingetrokken
Aantal pagina's 86
Commissie Anesthesie- en beademingssystemen
Gepubliceerd op 01-06-2009
Taal Engels
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PULSE OXIMETER EQUIPMENT intended for use on humans, hereafter referred to as ME EQUIPMENT. This includes any part necessary for NORMAL USE, including the PULSE OXIMETER MONITOR, PULSE OXIMETER PROBE, and PROBE CABLE EXTENDER. These requirements also apply to PULSE OXIMETER EQUIPMENT, including PULSE OXIMETER MONITORS, PULSE OXIMETER PROBES and PROBE CABLE EXTENDERS, which have been REPROCESSED. The intended use of PULSE OXIMETER EQUIPMENT includes, but is not limited to, the estimation of arterial oxygen haemoglobin saturation and pulse rate of PATIENTS in professional healthcare institutions as well as PATIENTS in the HOME HEALTHCARE ENVIRONMENT. This International Standard is not applicable to PULSE OXIMETER EQUIPMENT intended for use in laboratory research applications nor to oximeters that require a blood sample from the PATIENT. 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 relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 201.11 and in 7.2.13 and 8.4.1 of the general standard. This standard can also be applied to PULSE OXIMETER EQUIPMENT and their ACCESSORIES used for compensation or alleviation of disease, injury or disability. This International Standard is not applicable to PULSE OXIMETER EQUIPMENT intended solely for foetal use. This International Standard is not applicable to remote or slave (secondary) devices that display SpO2 values that are located outside of the PATIENT ENVIRONMENT.

Details

ICS-code 11.040.10
11.040.55
Nederlandse titel Medische elektrische toestellen - Speciale eisen voor basisveiligheid en essentiĆ«le prestaties van pulse oximeterapparatuur voor medisch gebruik - Deel 2-61
Engelse titel Medical electrical equipment -Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use - Part 2-61
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