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

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    syngo Application Software (VE21)

    FDA 510(k)
    FDA Class 2 ·Radiology

    KeyPrint

    FDA UDI
    Keystone Industries·H66842204331·KeyDenture Base Light Pink 1kg

    NEXT Coarse Orange Vanilla Prophy Paste Box 200

    FDA UDI
    Preventech·D024220433·NEXT Coarse Orange Vanilla Prophy Paste Box of ...

    FT101 FOREHEAD THERMOMETER; FT101 INFRARED DIGITAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLEAR + BRILLIANT LASER SYSTEM

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

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 23, 2026

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 3, 2025

    QT SCANNER 2000 MODEL A

    FDA Adverse Event
    Injury ·QT IMAGING HOLDINGS, INC.·Product code IYO·October 30, 2025

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 23, 2011

    SYNCRHOMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·November 4, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·July 1, 2025

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·December 1, 2023