Passed in 2012, the Medical Device Act (MDA) and the Medical Device Authority Act (MDAA) represent the first efforts by Malaysia to implement mandatory safety requirements for medical devices marketed or sold in that country. Regulations under the MDA replaced the country’s voluntary product registration scheme, originally established in 2006, and now require registration of all medical devices manufactured, imported or distributed in Malaysia. The law also provides suitable transition periods for manufacturers to register with the country’s newly established Medical Devices Authority.
To register a medical device for sale in Malaysia, a manufacturer must retain the services of a conformity assessment body (CAB) licensed by the Medical Device Authority to review and certify the registration application. As part of the conformity assessment process, the CAB will conduct a technical file review and an audit of the manufacturer’s quality management system. Certified applications are then submitted to the Medical Device Authority through an online registration system for final review and approval.
In addition to these requirements, manufacturers and importers must obtain an “establishment license” in order to legally market or sell medical devices in Malaysia. Manufacturers with no local presence in Malaysia are also required to appoint a Malaysia Authorised Representative, responsible for managing the device registration process and serving as the manufacturer’s legal representative in all dealings related to the review and approval of the device.
TÜV SÜD Malaysia is a licensed CAB under the MDA, and can conduct all review and assessment activities required to certify a device registration application. TÜV SÜD Malaysia can also conduct an audit of a manufacturer’s quality management system as part of the quality assessment process.
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