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

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    SPEEDLOCK HIP KNOTLESS FIXATION IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ArgenPMMA 98x30-B4

    FDA UDI
    ARGEN CORPORATION, THE·D818123240·Crown And Bridge, Temporary, Resin

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854015374·SMART PIN DIAMETER 3.2 X 40MM

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854015377·SMART PIN DIAMETER 3.2 X 40MM

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970577·

    3.7 MP COLOR LCD MONITOR, RADIFORCE MX270W

    FDA 510(k)
    FDA Class 2 ·Radiology

    ST AIA-PACK CA 19-9

    FDA 510(k)
    FDA Class 2 ·Immunology

    LINEAR? ST

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 27, 2026

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 20, 2025

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·February 22, 2021

    UNKNOWN NEXGEN LCCK TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 1, 2026

    UNKNOWN PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 30, 2026

    UNKNOWN NEXGEN LCCK FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 3, 2026

    UNKNOWN ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 31, 2026

    UNKNOWN TIBIAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 31, 2026

    UNKNOWN TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 31, 2026

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITJ·May 21, 2013

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FRN·September 26, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 14, 2011

    UNKNOWN FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 31, 2026