BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SmartLinx Vitals Plus Patient Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016531·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016517·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016500·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016494·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386417·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 10 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386431·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 9 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327385984·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 8 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386448·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 12 MM

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·May 2, 2025

    FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·May 2, 2025

    DUO-VENT CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·September 29, 2022

    CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·October 31, 2022

    CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·November 1, 2022

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 5, 2023

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IOR·June 20, 2013

    GEMSTAR 7 THERAPY

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·May 5, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code ITI·October 17, 2014