BEUDAMED
    37 results · 26ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Radiology

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074465074·CDH 7191530 HA COATED 5.5X30

    Phasix

    FDA UDI
    Davol Inc.·00801741107610·Phasix Mesh, 6" x 12" (15 cm x 30 cm), Rectangle

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365104107·

    EVOLUTION DUODENAL STENT SYSTEM, MODEL EVO-22-27-6-D, EVO-22-27-9-D, EVP-22-27-12-D

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

    BODYFIX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    SAGITTAL SAW-ATTACHMENT F/TRS

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWE·June 26, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code LFR·September 26, 2008

    PECTUS BLU PRBNT TI BAR 12IN

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·July 31, 2025

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·May 1, 2018

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MUM·November 16, 2017

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·November 12, 2014