Disclaimer
Any reference to a commercial product, process, service, or company is not an endorsement or recommendation by the Medical Device Branch, Therapeutic Products Division, Health Sciences Authority, or any of its components. Manufacturers and/or its Registrants shall ensure that the medical device listed in the Singapore Medical Device Register (SMDR) meets the essential requirements for safety, quality and performance and keep objective evidence to establish that the medical device continues to meet those requirements.
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Voluntary Product Registration Scheme (VPRS)
Any medical device registration application submitted to HSA before 31 March 2007 under the Voluntary Product Registration Scheme (VPRS) , were evaluated in accordance to VPRS requirements.
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TradeNet® Declaration Procedures for Medical Devices that are listed on Singapore Medical Device Register (SMDR)
HS Codes that are controlled solely by Medical Device Branch
This document provides the procedure to facilitate Import Permit applications via TradeNet® for medical devices listed on the Singapore Medical Device Register (SMDR) which use HS Codes that are controlled solely by MDB. Please refer to MDB Circular.
HS Codes that are Jointly Controlled by Medical Device Branch & other Controlling Agency (CAs)
This document provides the procedure to facilitate Import Permit applications via TradeNet® for medical devices listed on the Singapore Medical Device Register (SMDR) which use HS Codes that are Jointly Controlled by MDB and other controlling Agency (CAs). Please click here to refer to the document.
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