BEUDAMED
    15 results · 23ms · Sources: EU EUDAMED, US FDA

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    RADIFORCE RX240

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304213937·

    6000 NDGB

    FDA UDI
    HANS RUDOLPH, INC.·00817136021935·500 LITER NONDIFFUSING GAS BAG

    Plateau-C Ti

    FDA UDI
    Life Spine, Inc.·00190837066802·20mm x 16mm Graft Packing Tool

    REHASTIM 2, REHAMOVE 2

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYMBIA.NET

    FDA 510(k)
    FDA Class 2 ·Radiology

    PAGEWRITER TC 20 CARDIOGRAPH

    FDA Adverse Event
    Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC·Product code DPS·May 17, 2021

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    M2A 38MM MODULAR HEAD +3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2013

    LIFECARE PCA 3 V5.06

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·September 17, 2014

    VASOVIEW HEMOPRO 2 EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 17, 2011

    R3 XLPE INSERT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·May 25, 2025