BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    CUTTER, P607 BONE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00843471188330·.022 L/L STD. WELD SIZE #5

    PRE-LOADED VISICOIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Spinal Manometer NRFit; Spinal Manometer LUER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RECIPROC BLUE FILES, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·August 24, 2022

    ANGIOMAT ILLUMENA

    FDA Adverse Event
    Malfunction ·LIEBELFLARSHEIM COMPANY·Product code DXT·February 18, 2014

    ETRIO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·October 3, 2012

    UNKNOWN DEPUY PFC INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 21, 2010

    Exactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 38, 41, 44 head, Large, Item Number 314-13-04; Shoulder Arthroplasty

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