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

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    MiroTract Wound Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 60CM, REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 100CM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDELA PUMP IN STYLE ADVANCED BREAST PUMP

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

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 8, 2023

    6 SHOOTER SAEED MULTI-BAND LIGATOR

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC.·Product code MND·August 15, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 6, 2014

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 17, 2013

    ITREL II

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·May 19, 2014

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022