BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Titan Ag 200

    FDA 510(k)
    FDA Unclassified ·Unknown

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 1, 2025

    RADIFORCE RX240

    FDA 510(k)
    FDA Class 2 ·Radiology

    CHEMTRUE HCG PREGNANCY URINE DIPSTICK, HCG PREGNANCY URINE CASSETTE TEST, AND HCG COMBO SERUM/URINE CASSETTE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    COMPRESSION/DISTRACTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWN·August 28, 2020

    MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code INI·October 15, 2014

    AWL Ø14/3.2 CANN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWJ·June 17, 2013

    REGENEREX RINGLOC MULTI HOLE ACETABULAR CUP SZ 25 WITH LOCK RING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·July 24, 2011

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 14, 2014

    FT3 - FREE TRIIODOTHYRONINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·April 30, 2014