BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    IMMUNODOT MONO-M TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902959059·TRIAL 974-244 LORD 12X14X14

    SENSIDERM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DYNATECH MR 300 MANUAL MICROELISA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·February 14, 2013

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 31, 2011

    5MM, 45CM PEEK MULTI-FUNCTION HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code KOG·August 1, 2014

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023