BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Fixone Biocomposite Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Disposable Iris Retract

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114346·FLEXIBLE IRIS RETRACTORS 5 PKS of 5

    Harvey(R) Surgical Assistant

    FDA 510(k)
    FDA Class 2 ·Neurology

    ExsoMed INnate NanoTM Lag Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 6, 2008

    POLARIS 6.35/SYNERGY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·September 1, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013

    CADD

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·May 26, 2022

    AVALON US TRANSDUCER

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code HGL·May 31, 2024

    AVALON US TRANSDUCER

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code HGM·May 31, 2024

    AVALON US TRANSDUCER

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code HGL·February 18, 2025