BEUDAMED
    110 results · 28ms · Sources: EU EUDAMED, US FDA

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    DPX SERIES BRAVO DUO BONE DENSITOMETER

    FDA 510(k)
    FDA Class 2 ·Radiology

    Cusco Large w/Center Screw

    FDA UDI
    MEDGYN PRODUCTS, INC.·M803030962·Cusco Large w/Center Screw 1 3/8" x 4 1/2" (35m...

    Micro-Mega SA

    FDA registration
    Micro-Mega SA·7 products·🇫🇷 France

    PICO SMOKERLYZER, MODEL EC-50

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    EMIT II PLUS METHADONE ASSAY, MODEL OSRE229

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 21, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·January 9, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWP·January 21, 2010

    C21617 DE LIFE SYSTEMS $PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 24, 2013

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

    CD HORIZON

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 22, 2015

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·March 21, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·March 21, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 16, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 23, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWP·July 2, 2010

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·April 2, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 4, 2011