BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    29G AND 30G K-PACK II NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ClariFix Device

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

    GALAXY INTRAVASCULAR ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code IYO·February 14, 2013

    EVERCROSS

    FDA Adverse Event
    Malfunction ·EV3, INC.·Product code DQY·January 12, 2011

    CVC SET: 3-LUMEN 7 FR X 30 CM

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code FOZ·July 15, 2014

    Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025