BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PORGES CYTOLOGY BRUSHES

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756692953·GU TUR BASIN SET PGYBK

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867514508·Distraction-Compression Clamp

    NEOTECH MUCUS TRAP W/CATHETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·January 16, 2014

    HEMOSPLIT, 14.5 FR, STANDARD KIT, 19 CM, STRAIGH

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code MSD·December 28, 2012

    OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·June 26, 2024