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Another type of medical ID jewelry indicates membership in a medical information organization such as the MedicAlert Foundation, American Medical ID, and StickyJ Medical ID. Such medical ID jewelry includes a member identification number and a toll-free number or URL for medical emergency personnel to obtain full information about the wearer's ...
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Operate 51 CT Scans Centres (X-ray computed tomography), 64 Slice CT Scan Centers, 8 M.R.I Scans Centre (Magnetic resonance imaging), 2 Lithotripsy Centre, 7 Regional Diagnostic Centres (offers 68 different Diagnostic lab tests) and Master Health Checkup Centers at Tamil Nadu Government Medical Institutions & Hospitals
Barcode technology can help prevent medical errors by making accurate and reliable information readily available at the point-of-care. Information, such as the drug identification, medication management, infusion safety, specimen collection, etc. and any other patient care activity can be easily tracked during the patient stay.
The BIS Hallmark is a hallmarking system for gold as well as silver jewellery sold in India, certifying the purity of the metal. [1] [2] It certifies that the piece of jewellery conforms to a set of standards laid by the Bureau of Indian Standards, the national standards organization of India.
Medical device software that is an adjunct to another medical device and is involved in data manipulation, data analysis, data editing, image generation, determination of measurements, identification of a region of interest in an image, or identification (by an alarm or alert) of results from a monitor that are outside of an established range ...
The state enforced certification marks presently in India are (alphabetical list): Agmark: for all agricultural products. [2] [3]BIS hallmark: certifies the purity of gold jewellery.
The Unique Device Identification (UDI) System is intended to assign a unique identifier to medical devices within the United States, Europe, China, South Korea, Saudi Arabia and Taiwan. [1] It was signed into law in the US on September 27, 2007, as part of the Food and Drug Administration Amendments Act (Section 226) of 2007 .