BEUDAMED
    7 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.

    AUTO REFRACTOMETER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NORMCAP CD-102, CARBON DIOXIDE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OPUS MAGNUM IMPLANT SYSTEM, MODEL OM-1500

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOGIC CR TIB INSERT SLOPE +, SZ 3.5, 11 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 31, 2024

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code MDS·May 23, 2014

    UNKNOWN LEFT HIP

    FDA Adverse Event
    Injury ·STRYKER ORHTOPAEDICS MAHWAH·Product code JDI·November 2, 2012

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2010