BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    RESPONSE 5.5/6.0 Cannulated Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05714464010233·AO5 MNR T R MAC ALIGO 5 GPL

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM

    SMI CARDIOVASCULAR PATCH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed ExtremiFix Mini & Small System Tray

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2015

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·November 5, 2008

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 24, 2011

    UNKNOWN STEP DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SUR·Product code GCJ·July 1, 2013