BEUDAMED
    13 results · 35ms · Sources: EU EUDAMED, US FDA

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    CORELEADER HYDRO-HEALER HYDROCOLLOID WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    ArgenZ ST 98x12 ML OM3

    FDA UDI
    ARGEN CORPORATION, THE·D818123394·Dental porcelain/ceramic restoration kit

    BARCODE CONICAL COLLIMATOR VERIFICATION (BCCV)

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNISIGHT SYSTEM WITH UNIGATE

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 20, 2025

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·February 12, 2024

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·February 7, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·June 10, 2011

    BI-METRIC POROUS FMRL 10X130MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 17, 2018

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 17, 2018

    M2A-MAGNUM RECAP CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 17, 2018