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

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    SEGMENT

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoughAssist

    FDA UDI
    Respironics, Inc.·00606959021228·CoughAssist 70 Series Circuit, Adult Medium, 6ft

    AT WORK DRUG TEST, MODEL 9177T AWT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BOYD DELIVERY UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 2, 2013

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·September 15, 2014

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·April 26, 2011

    MILAGRO ADVANCE SCREW 7X23MM

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 16, 2019