BEUDAMED
    1,431 results · 23ms · 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.
    Filters Regulation: Us FDA ×

    OMNIPRO INCLINE

    FDA 510(k)
    FDA Class 2 ·Radiology

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252477464·DELTA 1.7MM CURVED PLATE 10 HOLE 0.5MM

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780243168·Titan™ Total Shoulder System The Titan Total Sh...

    NDO SURGICAL SURGICAL OVERTUBE

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

    BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910

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

    640G INSULIN PUMP MMT-1712K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·September 25, 2018

    CYLOS DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code DXY·May 3, 2013

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code GZB·August 27, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 18, 2011

    CONSERVE(R) PLUS SPIKED CUP

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KWA·February 8, 2016

    PROFEMUR(R) Z STEM PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LPH·February 8, 2016

    CONSERVE® PLUS SPIKED CUP

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code HWT·May 18, 2018

    CONSERVE® TOTAL A-CLASS® HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·May 18, 2018

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·January 3, 2019

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·July 9, 2018

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·April 8, 2018

    NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·February 9, 2018

    CONSERVE(R) PLUS SUPER FINISH FEMORAL

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code NXT·May 18, 2018

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KWA·May 18, 2018