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

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    PER-Q-CATH & PER-Q-CATH DUAL MUMEN CATHETERS, TRAYS & ACCESSORY DEVICES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150713·K-WIRE - SINGLE TROCAR 1.0mm DIA x 100mm

    IMMUCHEM V.I.P.(VISUAL INDICATED PREGNANCY)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ResScan Essentials

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ENPATH

    FDA Adverse Event
    Injury ·EXTERNAL MANUFACTURER·Product code NHW·January 10, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    PROTEUS XR/A

    FDA Adverse Event
    Malfunction ·GE HANGWEI MEDICAL SYSTEMS CO., LTD.·Product code KPR·November 15, 2007