BEUDAMED
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    BODYFIX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854014493·SMARTPIN SELF-REINFORCED TECHNOLOGY, Ø1.5 X 30 MM

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854014490·SMART PIN, DIAMETER 1.5 X 30MM

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930712153010·Custom 15" Curette #3/0 Ang Dark Blue handle

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321215300·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930712153000·Custom 15" Curette #3/0 Str Dark Blue handle

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311215300·

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180515013·PTP STYLE LIF INTRADISCAL SHIM, 30mm

    SafeGuide® Single

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734023235·Disposable Over the Guidewire Esophageal Dilato...

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

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

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

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

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

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

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code ESW·November 24, 2014

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694045414·PrimaLIF LLIF PEEK Implant, 15mm X 18mm X 30mm,...

    SIMPLICITY EASY P SOFT INFUSION SET FOR INFUSION AND/OR INJECTION OF FLUIDS INTO THE BODY BELOW THE SURFACE OF THE SKIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    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

    IH 15° Anatomic Abutment

    FDA UDI
    SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120484184·

    DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)

    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