BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    PIVOTAL SCISSOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Lacrimal Probe

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108741·BOWMAN LACRIMAL PROBE #0000-000

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code DXC·June 23, 2006

    µCor Heart Failure and Arrhythmia Management System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERIFY V-PRO CHEMICAL INDICATOR, VERSIONS 1 AND 2

    FDA 510(k)
    FDA Class 2 ·General Hospital

    WALLSTENT RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·March 21, 2025

    ASSY, PROBE, BLADDERSCAN BVI 9400/9600

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL·Product code IYO·February 15, 2013

    DXTEND GLENOSPHERE STD D38MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A·Product code KWS·January 26, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 1, 2014

    WALLSTENT? RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025

    NEBULAE I

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES INC.·Product code HIF·November 27, 2024