BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    CMOS Video-Rhino-Laryngoscope System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Bernafon

    FDA UDI
    Bernafon AG·05711584076033·CAPTO 9 FW 1.0

    ELASTIC BANDAGE CAT.#182-186 (WIDTH)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO PATHWAY PV ATHERECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FIBER DISK AND BLOCK

    FDA 510(k)
    FDA Class 2 ·Dental

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·June 29, 2018

    CRAGG-MCNAMARA

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·April 13, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 14, 2025

    2520274-2013-04616

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code OFB·August 27, 2013

    OPTICROSS?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code OBJ·October 17, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 14, 2013

    ALLURA XPER FD10

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·July 7, 2011

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 14, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 14, 2019

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 21, 2018

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 23, 2014

    ARROW DRAINAGE SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code GBX·December 20, 2020

    TRUE METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·February 9, 2024

    UNK - SCREWS

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·September 9, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 30, 2019