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Pre-market division & Post-market and enforcement division - CAB Unit

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CAB Unit

What is a CAB?

A body authorized by the Authority to perform specified conformity assessment activities to determine whether the relevant requirements in technical regulations or standards are fulfilled. CAB is independent of the organization that provides the product and is not a user of the product (3rd party) and Authority will monitor the performance of the CAB and, if necessary, withdraw authorization.

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  Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

  +603 - 8230 0300
  +603 - 8230 0200 
 

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  • Last Updated: 22 September 2023.
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