Announcement

Articles
Title	Published Date	Hits
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	07 January 2020	11807
GUIDANCE DOCUMENT : MDA/GD/0018: IMPORT AND/OR SUPPLY OF UNREGISTERED MEDICAL DEVICES FOR THE PURPOSE OF DEMONSTRATION FOR MARKETING OR EDUCATION	07 January 2020	14936
MEDICAL DEVICE (ADVERTISING) REGULATIONS 2019 AND MEDICAL DEVICE (DUTIES AND OBLIGATIONS OF ESTABLISHMENTS) REGULATIONS 2019	16 December 2019	23130
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 1 YEAR 2019 (REVISION 1) POST-MARKET RESPONSIBILITIES FOR MANUFACTURER AND AUTHORIZED REPRESENTATIVE (AR)	18 November 2019	14122
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	25 September 2019	12341
AWARENESS PROGRAM FOR NON-CORRECTIVE CONTACT LENS	24 September 2019	22653
MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION	17 September 2019	52387
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	28 July 2019	14457
Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE	22 July 2019	14888
DISCONTINUATION OF CONFORMITY ASSESSMENT BODY (CAB)	22 July 2019	10368

Title

Published Date

Hits

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

07 January 2020

11807

GUIDANCE DOCUMENT : MDA/GD/0018: IMPORT AND/OR SUPPLY OF UNREGISTERED MEDICAL DEVICES FOR THE PURPOSE OF DEMONSTRATION FOR MARKETING OR EDUCATION

07 January 2020

14936

MEDICAL DEVICE (ADVERTISING) REGULATIONS 2019 AND MEDICAL DEVICE (DUTIES AND OBLIGATIONS OF ESTABLISHMENTS) REGULATIONS 2019

16 December 2019

23130

CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 1 YEAR 2019 (REVISION 1) POST-MARKET RESPONSIBILITIES FOR MANUFACTURER AND AUTHORIZED REPRESENTATIVE (AR)

18 November 2019

14122

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

25 September 2019

12341

AWARENESS PROGRAM FOR NON-CORRECTIVE CONTACT LENS

24 September 2019

22653

MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION

17 September 2019

52387

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

28 July 2019

14457

Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE

22 July 2019

14888

DISCONTINUATION OF CONFORMITY ASSESSMENT BODY (CAB)

22 July 2019

10368

Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

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