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

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    FIXATOR PIN (EXTERNAL)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517311214·Archon Screw, 4.5x11mm S.T. Fixed

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78815111·Mini Sprint Bracket Roth .022" mand. 4 right

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756277273·Insulated Arthro Hook 45 Degree

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78815111001·Mini Sprint Bracket Roth .022" mand. 4 right

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78815110051·Mini Sprint Bracket Roth .022" mand. 4 right

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78815110101·Mini Sprint Bracket Roth .022" mand. 4 right

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575310074·Orthopaedic prosthesis implantation instrument,...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575310012·Orthopaedic prosthesis implantation instrument,...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575310036·Orthopaedic prosthesis implantation instrument,...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575310050·Orthopaedic prosthesis implantation instrument,...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575309979·Orthopaedic prosthesis implantation instrument,...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575309993·Orthopaedic prosthesis implantation instrument,...

    2.0 PK SUTURE ANCHOR T, 2.0 PK SUTURE ANCHOR S

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LECTROSWITCH MODEL E2502B

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

    PUMP MMT-722RNAP PRDGM INS PL EN RC

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·October 19, 2010

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·February 19, 2014

    CLARION IMPLANT

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·December 18, 2012