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

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    K-PACK SURSHIELD NEEDLE, HYPODERMIC NEEDLE FOR SINGLE USE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    JOBST ActiveWear

    FDA UDI
    BSN MEDICAL, INC.·00035664006006·ACTIVE WEAR 20-30 MM HG LARGE FULL CALF COOL WH...

    SYNTHES (USA) IMF SCREWS

    FDA 510(k)
    FDA Class 2 ·Dental

    HOVEROUND TEKNIQUE, MODEL HD-6

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 29, 2020

    OPERA

    FDA Adverse Event
    Malfunction ·ARJO MED AB LTD·Product code FSA·April 8, 2013

    PLUM A+ DRIVER NEW 8

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 16, 2014

    COBLATOR II

    FDA Adverse Event
    Malfunction ·ARTHROCARE ENT·Product code GEI·May 19, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2024

    BD SYRINGE 3ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 26, 2020

    LOGIC FEMORAL PS CEM LEFT SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 5, 2025

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 30, 2022

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 26, 2023

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 7, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 11, 2023