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

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    Ultrasound Scanner System bk2300

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016685·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016647·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016661·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016654·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386219·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 12 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386202·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 9 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386226·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 8 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386196·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 10 MM

    MIRAFLEX HIGH FLOW MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO: TRIO+SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DUO-VENT CLEARLINK LUER ACTIVATED VALVE

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

    AMISTEM P 01.18.409 AMISTEM-P STD STEM SIZE 9

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 25, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    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

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·October 15, 2014

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 20, 2013

    LS LF VENILOOP NON-DEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code FPK·May 5, 2011