Unique Device Identification (UDI) | Stryker
www.stryker.com › us › enThe U.S. Food and Drug Administration (FDA) created unique device identification, often abbreviated UDI, a rule that requires medical device manufacturers to update their products with a unique device identifier that includes both device and production identifiers (such as expiration date and lot or serial number).
Stryker Medical - Tech Web
techweb.stryker.comApr 14, 2022 · Navigate through the site by using the search box, navigation bar, or bread crumbs: Search by the product type, model number, then serial number range with the navigation bar on the left side. Navigate back to your search start by following your trail of bread crumbs at the top of each page. Send us your suggestions by clicking on the Feedback link in the upper right corner, please include your email address in your signature or in the body of your email otherwise we will not be able to respond.
International homepage | Stryker
www.stryker.com › us › enMedical and surgical equipment | Stryker Careers Investor Relations Patients Contact Are you sure you want to log out? If you choose to logout it will log you out from all the applications. CANCELLOG OUT About Medical and Surgical Equipment Orthopaedics Neurotechnology Services Care settings Training and Education Careers Investor Relations
www.stryker.com
www.stryker.com › us › enStryker - Medical Devices and Equipment Manufacturing Company | Stryker Careers Investor Relations Patients Contact Are you sure you want to log out? If you choose to logout it will log you out from all the applications. CANCELLOG OUT About Medical and Surgical Equipment Orthopaedics Neurotechnology Services Care settings Training and Education