BEUDAMED
    8 results · 20ms · 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 ×

    ENDOSERTER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450214992·

    POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SCANDINAVIAN IVF SCIENCES AB, GAMETE-100

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

    FLO-THRU INTRALUMINAL SHUNT

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DXC·May 2, 2013

    MITROFLOW AORTIC PERICARDIAL HEART VALVE

    FDA Adverse Event
    Death ·SORIN GROUP CANADA·Product code DYE·September 15, 2014

    HUMERAL NAIL 8X280 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·April 19, 2011

    INNOVANCE D-DIMER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code DAP·July 14, 2017