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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.
Stryker Corporation is an American multinational medical technologies corporation based in Kalamazoo, Michigan. [2] Stryker's products include implants used in joint replacement and trauma surgeries; surgical equipment and surgical navigation systems; endoscopic and communications systems; patient handling and emergency medical equipment; neurosurgical, neurovascular and spinal devices; as ...
FDA Rule Mandating Unique Device Identification for Reusable Medical Devices Creates New Market Opportunity for VeriTeQ in Breast Implant Sizers and Other Reprocessed ...
FDA Releases Final Rule for Unique Device Identification Final Rule Represents Significant Industry Shift to Use UDIs DELRAY BEACH, Fla.--(BUSINESS WIRE)-- Digital Angel Corporation ("Digital ...
A similar database is the Global Unique Device Identification Database (GUDID) of the FDA. As a key to EUDAMED, the MDR introduces the Basic UDI-DI as unique device identifier. A medical device (including system- and procedure packs and IVD) needs to have an assigned Basic UDI-DI and needs to be registered in the UDI/Device part of EUDAMED.
UDID is an acronym for Unique Device Identifier. The UDID is a feature of Apple's devices running iOS, tvOS, watchOS, and macOS. It is a unique identifier that is calculated from different hardware values, such as the ECID. It is sent to Apple servers when a user tries to activate the device during Setup.
In 2022, 6 years after Stryker's acquisition of Physio-Control, Stryker silently released the updated LIFEPAK 15 V4+ which featured the Stryker logo in place of the Physio-Control logo. [8] Alongside the release of this new model, all legacy Physio-Control websites (with the exception of " lucas-cpr.com ") were removed, with their URLs being ...
Global Medical Device Nomenclature (GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.