Categories
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12 Document Control - DCP-DOC-12/1Client Information Package 01/1-01/5ACT 737 & MDR 2012 DocumentsGuidance Document under Medical Device Act 2012 ( Act 737)General Medical Devices (GMD)In-Vitro Diagnostic (IVD) Medical Devices 03 Quality Policy10 Appeals and Disputes11 Complaints HandlingIndustry Engagement & FeedbackUseful Info
MDA/GD/0002 IN-VITRO DIAGNOSTIC (IVD) MEDICAL DEVICE CLASSIFICATION SYSTEM
In-Vitro Diagnostic (IVD) Medical Device Classification System
Second Edition
December 2020
