BEUDAMED
    23 results · 38ms · Sources: EU EUDAMED, US FDA

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    Arthrex NanoSuture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776163280·KNIFE HANDLE -LONG

    Super Upper Limbs Versalock Plating System

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663562·VERSALOCK RADIUS SHAFT PLATE, DORSOLATERAL ANGL...

    QMedix™

    FDA UDI
    Diagnostic Automation, Inc.·00850054026477·QMedix™Total Human IgE ELISA This test is inten...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011125·PedFuse RespondX, CNL, 6.0mm x 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011071·PedFuse RespondX, CNL, 6.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011118·PedFuse RespondX, CNL, 6.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011095·PedFuse RespondX, CNL, 6.0mm x 40mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011088·PedFuse RespondX, CNL, 6.0mm x 35mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011101·PedFuse RespondX, CNL, 6.0mm x 45mm

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973106876·TRIAL 90-SRK-180118 POLY PS 1X18MM

    TWIST DRILL

    FDA UDI
    Biomet Orthopedics, LLC·00887868017612·

    STIMTRODE SINGLE USE NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ZELTIQ AESTHETICS CLN1 DERMAL COOLING DEVICE

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

    NA

    FDA UDI
    STERILMED, INC.·10888551009447·DRILL BIT

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·February 16, 2018

    PERCUTANEOUS REFERENCE CROSS PIN FRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code MAX·April 24, 2019

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 17, 2014

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 4, 2013

    DREAMWIRE¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code EZB·July 27, 2011