BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194710·Interbody, 9mm x 32mm x 17mm, 8 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202705·Interbody, 9mm x 32mm x 17mm, 8 deg

    RHYTHM TOUCH Q 2-WAY

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MOSTDI DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    VERSYS FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·January 25, 2013

    TRILOGY LONGEVITY POLYETHYLENE LINER

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code JDI·December 14, 2010

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·July 14, 2014