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

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    BIOGEL NEOTECH II POWDER-FREE NEOPRENE SURGEON'S GLOVE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004184·CUSTOM PROCEDURE KIT

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004011·PowerChem Neoprene Exam Gloves, Extra Small

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282501877·TeWa CB-Type 2530 (s): uncoated acupuncture ne...

    TEWA

    FDA UDI
    asia-med GmbH·04251282509194·TeWa CB-Type 2530 (s): uncoated acupuncture ne...

    Contact glass 906 L

    FDA UDI
    Haag-Streit AG·07640132986396·

    Augurex

    FDA UDI
    Augurex Life Sciences Corp·00628425360020·14-3-3eta SRM POS H, 10-pack, ASR

    GentleMax

    FDA UDI
    Candela Corporation·00817495020570·Pulsed Laser

    Charcoal Output Filter

    FDA UDI
    I.C. MEDICAL, INC.·00817688021704·

    AESCULAP BONE WAX

    FDA 510(k)
    FDA Unclassified ·Unknown

    IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB

    FDA 510(k)
    FDA Class 2 ·Immunology

    VNS DEMIPULSE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·May 22, 2010

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 12, 2013

    ROTATABLE SNARE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FDI·February 22, 2008

    BONE WAX 24X2.5G

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·October 30, 2019

    EVIS EXERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·September 26, 2024

    BONE WAX 24X2.5G

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·May 7, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 15, 2019

    UNK DRILL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code HTW·November 15, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KXA·November 15, 2019