BEUDAMED
    39 results · 20ms · Sources: EU EUDAMED, US FDA

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    Ritter Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    MAESTRO TOTAL WRIST

    FDA UDI
    Biomet Orthopedics, LLC·00880304439085·

    Maestro™ Total Wrist

    FDA UDI
    Biomet Orthopedics, LLC·00887868239571·

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 17, 2022

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 17, 2022

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 17, 2022

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014669·PedFuse Respond, SLD, 7.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014751·PedFuse Respond, SLD, 7.0mm x 75mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014768·PedFuse Respond, SLD, 7.0mm x 80mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014744·PedFuse Respond, SLD, 7.0mm x 70mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014676·PedFuse Respond, SLD, 7.0mm x 35mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014690·PedFuse Respond, SLD, 7.0mm x 45mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014706·PedFuse Respond, SLD, 7.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014720·PedFuse Respond, SLD, 7.0mm x 60mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014737·PedFuse Respond, SLD, 7.0mm x 65mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014713·PedFuse Respond, SLD, 7.0mm x 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014683·PedFuse Respond, SLD, 7.0mm x 40mm

    MODEL MC-180MA MULTI-FREQUENCY BODY COMPOSITION ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONTROL SET DAT I, CONTRL SET DAT II, CONTROL SET DAT III, CONTROL SET AMPHETAMINE 1000 AND CONTROL SET AMPHETAMINE 500

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    QUIK-COMBO PACING/DEFIBRILLATION/ECG CABLE

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORPORATION·Product code LDD·August 6, 1997