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

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    HUMID-VENT FILTER PEDI

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150652·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 200mm

    ENDO-EASE ENDOSCOPIC OVERTUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Bencox M Stem (Bencox Hip System) and Bencox ID Cemented Stem (with Centralizer) & Bencox Bone Plug

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEE H10

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 17, 2020

    MEDI-LIFT

    FDA Adverse Event
    Other ·ARJOHUNTLEIGH MAGOG INC.·Product code FSA·June 19, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MILACA MANUFACTURING INC.·Product code LWP·February 9, 2013

    SIGN I. M. NAIL

    FDA Adverse Event
    Injury ·SURGICAL IMPLANT GENERATION NETWORK (SIGN)·Product code HSB·January 4, 2011

    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024