BEUDAMED
    19 results · 22ms · Sources: EU EUDAMED, US FDA

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    SurgiAid Collagen Wound Dressing (HA)

    FDA 510(k)
    FDA Unclassified ·Unknown

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517198129·MaXcess 4 Blade, 100mm Right

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776091552·Satinsky Vena Cava Clamp,

    LOCKING COLLET, TARGETING MODULE TIBIAL NAIL

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665013580·

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690121343·Femoral Augment Posterior, Size 2+, 10mm

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112700·BARRON VACUUM PUNCH 6.0MM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192923·10mm X 100mm Stem Pilot

    TEMPERATURE MODULE 242-100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Safecheck Gusseted Sterilization Reel(KR42100)

    Device
    EU MDR · Eu Md Class 1 ·Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.·On the market

    Safecheck Gusseted Sterilization Reel(KR42100-70)

    Device
    EU MDR · Eu Md Class 1 ·Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.·On the market

    Safecheck Gusseted Sterilization Reel(KR42100-3)

    Device
    EU MDR · Eu Md Class 1 ·Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.·On the market

    BLACKSTONE ASCENT POCT SYSTEM 5.5MM/3.0MM SINGLE AXIAL CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AIXPLORER

    FDA 510(k)
    FDA Class 2 ·Radiology

    Safecheck Gusseted Sterilization Reel (KR42100-70-3)

    Device
    EU MDR · Eu Md Class 1 ·Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.·On the market

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2023

    Biogran K244 100

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Biochem Bernburg GmbH·1 device

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013