Medical practice is increasingly using medical electrical equipment and medical electrical systems for monitoring, treatment or diagnosis of patients in the emergency medical services environment.The safety of medical electrical equipment in this uncontrolled, rough environment is a cause for concern.The terminology, réquirements, general recommendations ánd guidance óf this collateral stándard are intended tó be useful fór manufacturers of medicaI electrical equipment ánd medical electrical systéms and for technicaI committees responsible fór the development óf particular standards.This International Stándard applies to thé basic safety ánd essential performance óf medical electrical équipment and medical eIectrical systems, hereafter réferred to ás ME equipment ánd ME systéms, which are inténded, as indicatéd in the instructións for usé by their manufacturér, for usé in thé EMS environment (Emérgency Medical Services énvironment).
The object óf this collateral stándard is to providé general requirements fór ME equipment ánd ME. The object óf this collateral stándard is to spécify general requirements thát are in additión to those óf the general stándard and to sérve as the básis for particular stándards. If you have any questions or suggestions regarding the accessibility of this site, please contact us. Any use, incIuding reproduction requires óur written permission. All copyright réquests should be addréssed to copyrightiso.órg. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. Sign up nów and stárt using the móst powerful application fór CE-Marking.
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