BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Venture 0.014 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oticon

    FDA UDI
    Oticon A/S·05707131331465·OPN 2, KIT 10 NFM 85 C001

    Biogel

    FDA UDI
    Bosma Enterprises·10818634024159·Biogel Super-Sensitive Surgical 7.0 - 50 Pair/Box

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CENTRICITY CARDIO IMAGING

    FDA 510(k)
    FDA Class 2 ·Radiology

    PLUM XLM W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 14, 2013

    TERUMO CDI 100 MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·July 11, 2011

    ULTRAICE INTRACARDIAC ECHO CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code IYO·September 21, 2008

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·June 25, 2025