BEUDAMED
    8 results · 31ms · 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 ×

    LEEP REDIKIT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756349529·LAPAROSCOPY PACK

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

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REUSABLE TEST PACK FOR DANA EMULATING INDICATORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ETHICON PROLENE SOFT PRO MESH

    FDA Adverse Event
    Injury ·ETHICON·Product code FTL·January 9, 2013

    GENESISXP IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL- NEUROMODULATION·Product code LGW·November 18, 2010

    SPEEDBAND SUPERVIEW SUPER 7?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FHN·July 2, 2014

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015