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CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 2 YEAR 2018 (REVISION 2) : CONTROL OF ORPHANED, OBSOLETE AND DISCONTINUED MEDICAL DEVICE IN HOSPITAL, HEALTHCARE FACILITIES INSTITUTION OR ANY RELATED FACILITIES	Hits: 11037
GUIDANCE DOCUMENT : MDA/GD/0018: IMPORT AND/OR SUPPLY OF UNREGISTERED MEDICAL DEVICES FOR THE PURPOSE OF DEMONSTRATION FOR MARKETING OR EDUCATION	Hits: 14009
MEDICAL DEVICE (ADVERTISING) REGULATIONS 2019 AND MEDICAL DEVICE (DUTIES AND OBLIGATIONS OF ESTABLISHMENTS) REGULATIONS 2019	Hits: 20738
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 1 YEAR 2019 (REVISION 1) POST-MARKET RESPONSIBILITIES FOR MANUFACTURER AND AUTHORIZED REPRESENTATIVE (AR)	Hits: 13229
Unrecognise Training Provided By Other Parties Other Than Medical Device Authority In Relation To The Medical Device Act 2012 (Act 737) And Medical Device Regulatory Requirements	Hits: 11551
AWARENESS PROGRAM FOR NON-CORRECTIVE CONTACT LENS	Hits: 19196
MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION	Hits: 44713
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 2 YEAR 2018 REVISION 1 : CONTROL OF ORPHANED, OBSOLETE AND DISCONTINUED MEDICAL DEVICE IN HOSPITAL, HEALTHCARE FACILITIES INSTITUTION OR ANY RELATED FACILITIES	Hits: 13780
Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE	Hits: 13888
DISCONTINUATION OF CONFORMITY ASSESSMENT BODY (CAB)	Hits: 9499