BEUDAMED
    17 results · 24ms · Sources: EU EUDAMED, US FDA

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    Medilas H Laser Fibers

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

    THREADED STEINMANN PINS, DOUBLE END BAYONET POINT

    FDA UDI
    Biomet Orthopedics, LLC·00887868016608·

    EZ-CONNECT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RELINE-IT MODEL RELINE-IT

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·October 10, 2014

    TENSION FREE VAGINAL TAPE

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

    3.5FR P.U.R. UMBIL CATH X10

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·April 21, 2011

    PFC*SIGMA DIS AUG 8MM,SZ3,LEFT

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code JWH·February 21, 2014

    PFC SIGMA FEM POST AUG SZ3 4MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code JWH·February 21, 2014

    PFCSIG FLUT FEMROD 5DG14X175MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 21, 2014

    PFC SIGMA FEM POST AUG SZ3 4MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code JWH·February 21, 2014

    PFC*SIGMA C/S NPOR FEM LT SZ 3

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code JWH·February 21, 2014

    PFC SIGMA FEM STEM BOLT

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code JWH·February 21, 2014

    PFC*SIGMA DI AUG12MMCO,SZ3LEFT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 21, 2014

    PERSONA TRABECULAR METAL 2 PEG TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MBH·August 29, 2016

    BD¿ NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2019