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

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    Electric Wheelchair (JLE-W01A-2023)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    EarQ

    FDA UDI
    Sbo Hearing A/S·05714464053551·EARQ F20 MINIRITE R C093

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199649·Modular Knee Stem Pilot 25mm x 150mm

    Holder, Needle, TC, acc. Giannini 24cm

    FDA UDI
    Geister Medizintechnik GmbH·04057034065266·Holder, Needle, TC, acc. Giannini 24cm ...

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361023517·Ø12MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...

    POLYFLUX 14L, 17L, 21L HEMODIALYZER/FILTER LABELED FOR SINGLE USE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    STOP U (PACKED BLACK USA); STOP U (PACKED WHITE USA)

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

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 11, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 28, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 17, 2017

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 27, 2023

    INTERLINK CATHETER EXTENSION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·November 24, 2008

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 9, 2011

    9.5MM BORING TOOL,USE WITH XMAX ONLY

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·July 17, 2013

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 20, 2023

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 26, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 6, 2023