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

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    Filters Regulation: Us FDA ×

    AQUILION RXL

    FDA 510(k)
    FDA Class 2 ·Radiology

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·04026704099047·PERCUQUICK DILATOR SET, STERILE

    ESPIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINEFRONTIER LUMBAR IBF SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BATT F/NOS. 532.101+532.110

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·May 21, 2013

    FLEXI-SEAL FMS FECAL MANAGEMENT SYSTEM KIT

    FDA Adverse Event
    Malfunction ·CONVATEC, INC.·Product code KNT·July 29, 2014

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 2, 2011

    CONNECTA Q-SYTE WHT

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·February 19, 2019

    BD VACUTAINER® SODIUM FLUORIDE: 3 MG. NA2 EDTA: 6MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·April 30, 2019

    BD VACUTAINER® SODIUM FLUORIDE: 3 MG. NA2 EDTA: 6MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·March 18, 2019