BEUDAMED
    8 results · 30ms · Sources: EU EUDAMED, US FDA

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    Orchid Safety Release ValveTM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CIOS ALPHA

    FDA 510(k)
    FDA Class 2 ·Radiology

    PASSMED SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 21, 2025

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 7, 2008

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 1, 2011

    UNKNOWN DEPUY TIBIAL TRAY

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 17, 2013

    DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimens

    FDA Enforcement
    Class II ·Ongoing·Diasorin Inc.·December 18, 2024