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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
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Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE
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DISCONTINUATION OF CONFORMITY ASSESSMENT BODY (CAB)
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APPLICATION FOR NOTIFICATION OF EXPORT ONLY MEDICAL DEVICE
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NEW RELEASE GUIDANCE DOCUMENT MDA/GD/0051:GUIDANCE DOCUMENT ON NOTIFICATION OF EXPORT ONLY MEDICAL DEVICE
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PELETAKAN DALAM PASARAN DAN PENGGUNAAN PERANTI YANG TIDAK BERDAFTAR DAN TIDAK MEMPUNYAI BUKTI KLINIKAL
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CIRCULAR LETTER NO. 4 YEAR 2018 (REVISION 1) : EXEMPTION FROM REGISTRATION REQUIREMENT FOR EXPORT ONLY MEDICAL DEVICE
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CIRCULAR LETTER NO.2 YEAR 2016(REVISION 1) : MEDICAL DEVICE PROCUREMENT FOR HEALTHCARE INSTITUTION
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CIRCULAR LETTER NO.4 YEAR 2014(REVISION 1) : MEDICAL DEVICE FOR IMPORT/EXPORT FROM / TO COUNTRIES WITHOUT DIPLOMATIC TIES WITH MALAYSIA
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PENGUMUMAN BERKAITAN PERMOHONAN PENDAFTARAN PERANTI PERUBATAN DAN PERLESENAN ESTABLISMEN DI BAWAH AKTA PERANTI PERUBATAN 2012 (AKTA 737) YANG MASIH TERTANGGUH SETELAH TAMAT TEMPOH PERALIHAN
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Introduction
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Integrity Unit
Secretarial Unit
Pre-Market Control Division
Post Market & Enforcement Division
Policy & Strategic Planning Division
International and Industry Affairs Division
Management and Service Unit
FAQ
Single License Policy Implementation
Registration, Licensing & Enforcement
Labelling of Medical Devices
Technical Evaluation
Contact Us
Customer Complaint Form
Customer Satisfaction Survey
Staff Directory
Documents
Legislation
Circular Letter
Guidance Document
Guideline
Standard
General Directions
Strategic Plan
Slide Presentation
Infographic
Organizational Anti Corruption Plan (OACP) MDA 2022 - 2026
Buletin MDA
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Customer Satisfaction Survey Result
Annual Report
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