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

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    Riptide Aspiration System React 68 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002312·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002299·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002282·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000912·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000936·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000929·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002305·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002329·MCK Onlay Tibial Insert

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486002336·MCK Onlay Tibial Insert

    BONASTENT® Tracheal/Bronchial

    FDA UDI
    Sewoon Medical Co., Ltd.·08806369469043·

    ZYNO Z-800 INFUSION SYSTEM MODEL Z-800

    FDA 510(k)
    FDA Class 2 ·General Hospital

    APNEA RISK EVALUATION SYSTEM (ARES)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 24, 2024

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·May 29, 2019

    TROPONIN T STAT (SHORT TURN AROUND TIME)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·June 15, 2015

    KYPHON HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 29, 2019

    KYPHON HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·June 6, 2019

    KYPHON HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·September 20, 2019

    KYPHON HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 15, 2019