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

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    Deltaven XiV Max, Deltaven XiV Max FF

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694045766·PrimaLIF LLIF PEEK Implant, 15mm X 26mm X 30mm,...

    Canaveral®

    FDA UDI
    FLOSPINE LLC·B183117150300·Closed Screw Assembly, 10.5mm x 30mm

    KARL STORZ VIDEO FLEXIBLE VIDEO ENT ENDOSCOPE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    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

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 30, 2026

    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

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 24, 2026

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DTQ·June 24, 2011

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·September 17, 2008

    OPTIPAC 80 REFOB PLUS BONE CMT-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2026

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KNW·March 12, 2026

    REFOBACIN BONE CEMENT R 2X40G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MBB·March 12, 2026