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

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    CancelleX Porous Titanium Lumbar Interbody Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517576279·CoRoent Ant TLIF Ti, 9x10x36mm 4°

    CETRA

    FDA UDI
    Orthofix US LLC·18257200120581·3-LEVEL PLATE ASSEMBLY, 64MM

    GAMBRO CARTRIDGE BLOOD SET LOW WEIGHT- LOW VOLUME, MODEL 003422-520

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATURE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GORILLA/BABY GORILLA PLATING SYSTEM

    FDA Adverse Event
    Injury ·PARAGON 28, INC·Product code HRS·September 17, 2020

    UNKNOWN DEPUY HIP STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·October 3, 2008

    M2A-MAGNUM PF CUP 48ODX42ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 26, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·August 4, 2011