BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CATHETER, UMBILICAR ARTERY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771048746·K-Wires, Double trocar, .035-inch (0.9mm) diame...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292374·

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659483927·K-Wire w. double end trocarpoint _x000D_...

    K-Wire w. double end trocarpoint 0.90mm/152mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM710220·K-Wire w. double end trocarpoint 0.90mm...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776353490·Bone Impactor

    POWDER-FREE VINYL EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Ablation Confirmation

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRISM 6 CHANNEL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·October 3, 2012

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·December 18, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 14, 2015