BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    CRANIOPLUG

    FDA 510(k)
    FDA Class 2 ·Neurology

    Bernafon

    FDA UDI
    Bernafon AG·05711584052341·JU9 ITED, WL R BE JUNA 9

    INTREPED, Intraosseous Fusion Device

    FDA UDI
    Auxano Medical LLC·00850055649194·INTREPED 09 Sizer

    ADSON TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023550·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE SERR...

    BONASTENT® Tracheal/Bronchial

    FDA UDI
    Sewoon Medical Co., Ltd.·08806369468602·

    DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-1862

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FOB ONE STEP RAPID TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    LOGIC FEMORAL PS POR RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

    LOGIC CR FEMORAL POR, LEFT, SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEATHCARE CORPORATION·Product code KDI·October 3, 2014

    UNKNOWN NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·May 31, 2013

    TOTAL ASR FEM IMP SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JDG·October 9, 2015

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023

    LOGIC CR FEMORAL POR, RIGHT, SZ 3

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 14, 2019