BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OBSIDIAN PRESS (ALL CERAMIC AND POM)

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES (USA) 1.0/1.22 MM CRANIOFACIAL SCREWS

    FDA 510(k)
    FDA Class 2 ·Dental

    CONFIDENT SURGERY SUITE 300, MODEL CSS300

    FDA 510(k)
    FDA Class 1 ·Radiology

    ORTHOSIS,PEDICLE SPINAL FIXATION

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·December 8, 2015

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 5, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 28, 2011

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 25, 2015