BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    NuVasive Cohere ALIF System Intervertebral Body Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    DEPUY (IRELAND)·10603295523420·TRIAL HEAD DUAL MOBILITY REMOVAL TOOL 22.225MM ...

    CAPTURE-R READY INDICATOR RED CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·January 31, 2012

    ALTAIRE MAGNETIC RESONANCE IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPTURE-R SELECT

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·January 10, 2012

    SUN TIBIA Ø10 L345 SST

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code JDS·February 26, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2025

    RESERVOIR 1.8ML

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·November 3, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 24, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

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