BEUDAMED
    72 results · 29ms · Sources: EU EUDAMED, US FDA

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    HYSTALOG HSG CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832024728·GLENOID SIZER

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700003400·

    PedFlex Flexible Nailing System

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132100080·Ø4.0 MM X 450 MM FLEXIBLE IM NAIL

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520003400·Curved Ti Rod, 340mm

    Midmark

    FDA UDI
    MIDMARK CORPORATION·00841709105814·IQvitals Zone, Wireless Monitor, with Serenity ...

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700003400·

    MCGRATH

    FDA Adverse Event
    Malfunction ·AIRCRAFT MEDICAL LIMITED·Product code CCW·March 19, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·AIRCRAFT MEDICAL LIMITED·Product code CCW·March 19, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·AIRCRAFT MEDICAL LIMITED·Product code CCW·March 19, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·March 19, 2026

    INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CLINI-DENT

    FDA 510(k)
    FDA Class 1 ·Dental

    MCGRATH

    FDA Adverse Event
    Malfunction ·AIRCRAFT MEDICAL LIMITED·Product code CCW·March 19, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·November 7, 2025

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·March 23, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·March 23, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·March 23, 2026

    MCGRATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code CCW·November 7, 2025

    I-STAT ACTK (KAOLIN) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE CANADA LTD.·Product code JBP·May 31, 2011