BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    EARLYSENSE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MP Reconstruction System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575397709·Orthopaedic implant inserter/extractor, reusabl...

    DYONICS VISION 325Z DV3-CCD HERMES READY CAMERA SYSTEM, MODEL 7209531

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EQUINOXE UHMWPE 12* POSTERIOR AUGMENT PEGGED GLENOID, SMALL / MEDIUM / LARGE / EXTRA-LARGE, LEFT / RIGHT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·November 2, 2017

    APPOSE ULC 35 WIDE SKIN STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code GDT·May 13, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 1, 2014

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

    COBAS 6000 C (501) MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 16, 2016