BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    KAHN-TACT U.S.A., EFF LARYNGOSCOPE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Lacrimal Probe

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108673·MIYAKE LACRIMAL PROBE SET OF 5

    icotec Interbody Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GENERATION 8 SE ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    BATTERY 14.8V, 6.3 AH LI-LON BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 27, 2014

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 8, 2010

    DISPOSABLE SUTURE PLACEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code GCJ·December 13, 2012

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026