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

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    Filters Regulation: Us FDA ×

    PREVENA DUO, PREVENA PLUS DUO Incision Management Systems with PEEL & PLACE Dressings

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

    ABL90

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EXCEL CONTRA ANGLE HANDPIECE

    FDA 510(k)
    FDA Class 1 ·Dental

    ORTHOSIS,PEDICLE SPINAL FIXATION

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

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 11, 2013

    PINN LNR CON +4 10D 32IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWZ·July 11, 2011

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 10, 2014

    STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·January 10, 2019

    PLATE ADAPTER DIST. LAT. FEMUR RIGHT

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HWC·May 11, 2017

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

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