BEUDAMED
    9 results · 19ms · 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.

    PAPANICOLAOU STAIN SYS HT40

    FDA 510(k)
    FDA Class 1 ·Hematology

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127021053·Quick Connect Cup Trial Size 54

    Sterilizer, Soft-Lens, Thermal, Ac-Powered

    FDA Pre-Market Approval
    FDA Class 2 ·MODEL NO. ALS-IV HEAT DISINFECTION UNIT

    RESCAN

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GEENEN PANCREATIC STENT SET

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·July 16, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·November 20, 2012

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 15, 2010