BEUDAMED
    11 results · 23ms · 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 ×

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code DXC·June 23, 2006

    HEARTPORT ENDOAORTIC CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ROUND FILTERS W/INDICATOR

    FDA Adverse Event
    Malfunction ·SPS MEDICAL·Product code FRG·February 28, 2014

    Non-Sterile, Powder-Free, Nitrile Examination Gloves, Blue

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AESCULAP STERILCONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCLEAR LTD·Product code MCM·February 14, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·January 4, 2011

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZF·July 14, 2014

    BA102

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 31, 2016

    BA105

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 28, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·August 29, 2017