BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BioZorb SP Marker

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

    LOGIQ P3

    FDA 510(k)
    FDA Class 2 ·Radiology

    SWIFT-LOCK ANCHOR, MODEL 1192

    FDA 510(k)
    FDA Class 2 ·Neurology

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    SWIFT-LOCK ANCHOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 23, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 22, 2014

    TECNIS 1-PIECE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·August 4, 2011

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MHY·June 27, 2013

    MEDTRONIC TRANSCATHETER DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NPT·October 31, 2025

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·October 30, 2025

    FREESTYLE LIBRE 14 DAY

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC·Product code PZE·September 5, 2023

    FREE STYLE LIBRE 2

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC.·Product code QLG·June 10, 2022