BEUDAMED
    8 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 ×

    PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Family Wellness

    FDA UDI
    Family Dollar Stores·00032251058165·Extra Large Sheer Adhesive Bandages, all one si...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450217184·

    ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LAGLOVE BRAND COLORED POWDERED NITRILE EXAMINATION GLOVES(GREEN/PURPLE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 11, 2013

    MIRA CR4000 OPHTHALMIC CRYO UNIT

    FDA Adverse Event
    Malfunction ·MIRA, INC.·Product code GEH·November 23, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 2, 2014