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Samples in periodicals archive:
E-labelling will only be for devices exclusively used by professional users (home use devices will not be covered) and applicable to Medical Devices Directive 93/42/EEC (as amended by 2007/47/EC) and Active Implantable Medical Devices Directive 90/385/EEC.
In the UK, ALTs are regulated by the Medical Devices Directive ("MDD") and the Active Implantable Medical Devices Directive ("AIMDD").
The three medical device directives are part of the New Approach: MDD 93/42/EEC; Active Implantable Medical Devices Directive AIMDD 90/385/EEC; and In Vitro Diagnostic Directives 1VDD 98/79/EC.