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VeriTeQ's Q Inside technology can help medical device manufacturers comply with FDA Proposed Rule for UDI Direct Mark Requirement

VeriTeQ's FDA-cleared Q Inside microchip provides Automatic Identification and Data Capture technology as required under FDA’s Proposed Rule.

Scott Silverman, Chairman and CEO, noted, "Our “Q Inside” technology not only can help device manufacturers, but ultimately can enable a patient’s healthcare team to have accurate and timely access to data about an implantable medical device, in vivo, on demand, in the event of a recall or other safety event. We are not aware of any other currently available and proven technology that has this ability.”

Read the full release online, and visit VeriTeQ's web site for more information about this technology.

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