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Guidance Documentshttps://portal.mda.gov.my/index.php/doc-list/guidance-document
Guidance Document under Medical Device Act 2012 (Act 737) These Guidance Documents were prepared by the Medical Device Authority (MDA) to help the industry and healthcare professionals in their quest to comply with the Medical Device Act (Act 737) and...
PRODUCT CLASSIFICATION Product Classification Application: To determine whether the product is classified as a medical device or non-medical device product by the definition of medical device under Act 737. *Note:- Product Classification is not...
This Guidance Document was prepared by the Medical Device Authority (MDA) to help the industry and healthcare professionals in their quest to comply with the Medical Device Act (Act 737) and the regulations under it. This Guidance Document will be...