BEUDAMED
    7 results · 36ms · Sources: EU EUDAMED, US FDA

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    Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V4.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    BABY QUASAR

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

    FLEXI-Q DV AND DVR AUTO-INJECTORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 26, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 25, 2008

    CERTAS INLINE VLV W/ SPHNGRD

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·January 5, 2022