TREATMENT OF COMPUTERS USED TO PROGRAM IMPLANTABLE PULSE GENERATORS
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GUIDELINES RELATING TO THE APPLICATION OF : THE COUNCIL DIRECTIVE 90/385/EEC ON ACTIVE IMPLANTABLE MEDICAL DEVICES THE COUNCIL DIRECTIVE 93/42/EEC ON MEDICAL DEVICES
Document status: [ Active ]
GUIDELINES RELATING TO THE APPLICATION OF : THE COUNCIL DIRECTIVE 90/385/EEC ON ACTIVE IMPLANTABLE MEDICAL DEVICES THE COUNCIL DIRECTIVE 93/42/EEC ON MEDICAL DEVICES
Document status: [ Revised ]
GUIDELINES RELATING TO THE APPLICATION OF: THE COUNCIL DIRECTIVE 90/385/EEC ON ACTIVE IMPLANTABLE MEDICAL DEVICES THE COUNCIL DIRECTIVE 93/42/EEC ON MEDICAL DEVICES
Document status: [ Active ]
GUIDELINES RELATING TO THE APPLICATION OF: THE COUNCIL DIRECTIVE 90/385/EEC ON ACTIVE IMPLANTABLE MEDICAL DEVICES THE COUNCIL DIRECTIVE 93/42/EEC ON MEDICAL DEVICES
Document status: [ Active ]
GUIDELINES ON THE QUALIFICATION AND CLASSIFICATION OF STAND ALONE SOFTWARE USED IN HEALTHCARE WITHIN THE REGULATORY FRAMEWORK OF MEDICAL DEVICES
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LIST OF BODIES NOTIFIED UNDER DIRECTIVE 901385/EEC Active implantable medical devices
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DESIGNATION AND MONITORING OF NOTIFIED BODIES WITHIN THE FRAMEWORK OF EC DIRECTIVES ON MEDICAL DEVICES
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GUIDELINES ON MEDICAL DEVICES APPLICATION OF COUNCIL DIRECTIVE 93/42/EEC TAKING INTO ACCOUNT THE COMMISSION DIRECTIVE 2003/32/EC FOR MEDICAL DEVICES UTILISING TISSUES OR DERIVATIVES ORIGINATING FROM ANIMALS FOR WHICH A TSE RISK IS SUSPECTED
Document status: [ Revised ]
