BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    HISTOFREEZER

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

    SwishPlus® Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106166·Ø3.7 x 8 Platform 3.5mmD

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113874·PS-R Insert, Size 1 x 14mm

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981205393·Trial, 9mm x 24mm x 11mm, 5 Deg

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123083·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 100mm

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981286354·Interbody, 9mm x 24mm x 11mm, 5 Deg, 3D

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981191252·Interbody, 9mm x 24mm x 11mm, 5 Deg

    A-SCAN 100

    FDA 510(k)
    FDA Class 2 ·Radiology

    ANATECH X-RAY GENERATOR

    FDA 510(k)
    FDA Class 1 ·Radiology

    UNKNOWN DEPUY METAL LINER

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ? REG. # 8010379·Product code JDI·January 22, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·December 14, 2010

    OPTISENSE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014