BEUDAMED
    11 results · 28ms · 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 ×

    KIMBERLY-CLARK INTRODUCER KITS

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

    RMO

    FDA UDI
    Rmo, Inc.·00885797099754·LING RETNR BOND 4X4 6 CASE KIT

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221024848·Unitek(TM) Lingual Sheaths Slotted Tube UL/LR M...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450179376·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450184882·

    SILENT NIGHT V

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FORTIFY DR, DF4 CONNECTOR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·April 26, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code FPA·April 6, 2011

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 22, 2008

    HANDLE CEV102910R DIA 10MM ANG W/RATCHET [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GCJ·December 20, 2013