BEUDAMED
    6 results · 17ms · 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.

    UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    CK10000 SERIES POUCH & BAGS ETC.

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SHUTT PRECISION PROBES

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·November 16, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·September 23, 2010