BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SCI-PRO, PROPHYLAXIS PASTE

    FDA 510(k)
    FDA Class 1 ·Dental

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209136155·

    Multiphase Blue ChromiumCobalt

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746050367·WIRE SS MULTIPHASE LOWER 018 X 022 BONWILL HAWL...

    WIRE, GUIDE - MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IRRADIATOR FOR BIOLOGICAL MATERIALS IBL-437-C

    FDA 510(k)
    FDA Unclassified ·Unknown

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2014

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 3, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021