BEUDAMED
    10 results · 33ms · 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 ×

    TROKAMED GMBH ENDOSCOPES AND ACCESSORIES

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

    Mini-Mono® Brackets

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70602331·Mini-Mono-Brackets Andrews 'N' .018" 1000 Brackets

    PROTOS DR/CLS

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DXY·November 3, 2006

    SELOX SR 45

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·November 3, 2006

    MENICON SF-P

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    POWDER FREE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HOURGLASS

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MQP·June 16, 2014

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 11, 2013

    CRE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·April 15, 2011

    INJECTION GOLD PROBE BIOPLAR CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·June 12, 2008