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

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    COAGULATION CONTROL LEVEL 3 (ABNORMAL)

    FDA 510(k)
    FDA Class 2 ·Hematology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984131·anteriors; shade A3; mould 99

    Trinias

    FDA UDI
    SHIMADZU CORPORATION·04540217058754·

    DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WILTEK ELECTROCAUTERY ADAPTOR

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

    OPTETRAK LOGIC KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 24, 2024

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 28, 2013

    COLLEAGUE 3 CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 10, 2011

    SUPER SUCKER SHORT CURVED (BX/20)

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 27, 2024

    LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 29, 2022