BEUDAMED
    7 results · 27ms · 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.

    INTRAVASCULAR CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    *

    FDA Adverse Event
    Injury ·DOW CORNING CORP.·Product code FTR·March 18, 1997

    ABL90 FLEX ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AURORA DS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VASOVIEW 7 XB

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 7, 2014

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·November 14, 2012

    TRABECULAR METAL GLENOSPHERE HELMET

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSD·September 7, 2010