BEUDAMED
    12 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    ENZYME IMMUNOASSAY ANTI-SM ANTIBODY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517840806·XLIF XL Paddle Sizer, 10mm Bullleted

    FIXOS

    FDA UDI
    Stryker GmbH·07613327083200·Drawer Tag - 4.0,5.0 mm Instruments

    3M™ ESPE™

    FDA UDI
    3M COMPANY·30605861031210·3M™ ESPE™ Gold Anodized Crown Refills, First Bi...

    STERLING

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975065247·

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690191391·Patella Resection Cover Size 38

    VASCULAR SOLUTIONS D-STAT DRY 3X3 HEMOSTATIC PAD

    FDA 510(k)
    FDA Unclassified ·Unknown

    MIROMATRIX WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·December 21, 2010

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Death ·MPRI·Product code LWS·July 17, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 19, 2012

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024