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Standardization in the field of non-active medical devices with the objective to identify, adopt or adapt ISO or other standards, or if no ISO or other standard exists, to prepare CEN standards relevant to the Medical Device Directive for non-active medical devices. Excludes equipment currently within the scopes of other CEN/TC, but includes (with appropriate liaison with CENELEC) some types of equipment that use electrical power (from battery or mains supply) for functioning.
