The Medical Devices Branch of Singapore’s Health Sciences Authority (HSA) is seeking public comment on draft guidance, issued on 25 May, that aims to provide clarity on regulatory requirements for Singapore’s new Unique Device Identification (UDI) system.
A standardized product identification code and a system to track devices throughout the supply chain and health care system will aid device traceability and timely identification of specific devices and patients involved in recalls, device failures or serious adverse events, said the HSA
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