BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    STERILIZATION PROCESS/VAGINAL SPONGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    TLX

    FDA UDI
    Nuvasive, Inc.·00887517825179·TLX Implant, 12x11x31mm 20°

    ENTERAL FEEDING TUBE AND ACCESSORIES, FEEDING TUBE EXTENSION SET

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

    LOMBARD-DOWELL NECMYCIN EGG YOLK AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 20, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 16, 2012

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2010

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

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