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

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    SEASPINE VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809849912·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE LARGE FU...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192190·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...

    MODEL 9000 PEDIATRIC WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DIGORA PCT

    FDA 510(k)
    FDA Class 2 ·Dental

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·November 28, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 6, 2021

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·May 22, 2018

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·April 11, 2013

    ENDEAVOR RESOLUTE RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·March 1, 2011

    PD1200 DEFIBRILLATOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LDD·May 20, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·April 21, 2020