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EN 62353:2014 Medical electrical equipment. Recurrent test and test after repair of medical electrical equipment; Moreover, there are a lot of ISO and IEC standards that were accepted as "European Standard" (headlined as EN ISO xxxxx) and are valid in the European Economic Region.
European standards are generally annotated by the organization, standard number and year of publication (e.g. CEN 1789:2000 or CEN 1789/2007). Within member countries, [ 2 ] the annotation is likely to be adapted to include the local standards body, so that in Britain, the 'C' is dropped from the prefix, and replaced with ' BS ', in Germany ...
ESC – European Society of Cardiology; ESH – European Society of Hypertension; ISH – International Society for Hypertension; ISHIB – International Society for Hypertension in Blacks; JNC – Joint National Committee; KDIGO – Kidney Disease: Improving Global Outcome
The European respirator standards refer to the filtering classification by EN 149, EN 14683, and EN 143, all European standards of testing and marking requirements for respirators. [1] FFP standard masks (where FFP stands for filtering facepiece) [ 2 ] cover the nose, mouth and chin and may have inhalation and/or exhalation valves.
The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the ...
European accreditation through UEMS-EACCME [6] means that a CME activity, event, program or e-learning material has fulfilled the UEMS-EACCME quality requirements. . Accreditation will only be provided if the CME activity or material has a high quality scientific content and an appropriate educational approach, and if it is a free of comm
EN 207 is a European norm for laser safety eyewear (now superseded, together with the EN 208, by the ISO 19818:2021 standard [1]). Any laser eye protection sold within the European Community must be certified and labeled with the CE mark. According to this standard, laser safety glasses should not only absorb laser light of a given wavelength ...
European Standards must be transposed into a national standard in all EU member states. This guarantees that a manufacturer has easier access to the market of all these European countries when applying European Standards. Member countries must also withdraw any conflicting national standard: the EN supersedes any national standard.