BEUDAMED
    10 results · 26ms · 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.

    AQUEOUS BLOOD GAS CONTROL LEVEL I,II &

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8320031·DD cube ONE® ML are dental mill blanks made fro...

    WILSON PLATELET HOLDING INSTRUMENT 11MM WIDE

    FDA UDI
    W.H. Holden, Inc.·D9288320030·

    PREMIER PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    WINX SLEEP THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    2.3MM X 22MM NON-TOGGLING CORTICAL SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·February 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 14, 2012

    HEART START XL

    FDA Adverse Event
    Injury ·PHILIPS HEALTHCARE·Product code MKJ·September 8, 2010

    FREESTYLE LITE

    FDA Adverse Event
    Injury ·Product code NBW·August 18, 2011