The U.S. Food and Drug Administration (FDA) categorizes medical devices into three classes based on the level of risk the devices pose to patients and users. Image Credit: IGORdeyka/Shutterstock.com ...
A medical device is any appliance, apparatus, software, material, or other articles, which may be used in isolation or combination (as defined by the manufacturer) by individuals for a medical purpose ...
In order to implement the new Medical Device (MD) Rules, the Gujarat Food and Drug Control Administration (FDCA) has notified 145 MD officers to inspect Class A and Class B medical device ...
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