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SUMMARY OF MEDICAL DEVICE-DRUG-COSMETIC INTERPHASE (MDDCI) PRODUCT CLASSIFICATION DECISION
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RECALL : VOLUNTARY RECALL OF DUREX REAL FEEL BATCH
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PENGUMUMAN BERKENAAN PENGGUNAAN LOGO DAN NAMA PIHAK BERKUASA PERANTI PERUBATAN
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LICENSE CONDITION FIRST REVISION
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CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 4 YEAR 2017
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CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY
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GUIDANCE DOCUMENT ON REQUIREMENTS FOR EXPORT PERMIT
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NEW CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 3 YEAR 2017 (IMPLEMENTATION AND ENFORCEMENT
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Guidance Document on Notification of Exemption from Registration of Medical Devices for the Purpose
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CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 3 YEAR 2017
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Home
Introduction
Background
Vision, Mission & Core Value
Functions
Contact Us
Organisation Chart
Code of Ethics and Conduct
Board of Directors
Top Management
Division
Chief Executive's Office
Corporate Communication Unit
Legal Unit
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
Press Release
Media Coverage (Newspaper Cutting)
Customer Satisfaction Survey Result
Annual Report
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