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- W2039448163 abstract "The two standards to which medical lasers should be designed are IEC 601-1 (Medical Electrical Equipment, Part 1 General Requirements) and IEC 825 (Radiation Safety of Laser Products, Equipment Classification Requirements and User's Guide). These standards do not cover all the requirements so there is a Part 2 to IEC 601-1 being produced which also relates to IEC 825 which supplements, amends or deletes clauses in both main documents as applicable. This Part 2 is not expected to be available until August 1990 so until then it is the two main standards which should be applied as far as possible by manufacturers and test houses. With 1992 only two years away the European Community is trying to produce standards for use within the Community after that date. Clearly, to utilize existing standards from some member countries has attractions from an efficiency standpoint but it does mean that other countries have not had the opportunity of contributing to the standard and are presented with a fait accompli. A number of European countries are therefore fielding very strong teams of representatives to standards meetings to try and get their standards accepted as the European Norm. IEC 601-1 has just been revised and a 1988 edition is available but the 1977 edition is still in force, IEC 825 is undergoing revision so the position so the position is rather fluid. It is recommended that manufacturers design their equipment to the latest edition as there will be a changeover period during which both old or new standards are acceptable." @default.
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- W2039448163 date "1989-08-01" @default.
- W2039448163 modified "2023-09-25" @default.
- W2039448163 title "Laser standards for medical purposes" @default.
- W2039448163 doi "https://doi.org/10.1016/0030-3992(89)90085-6" @default.
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