BEUDAMED
    7 results · 24ms · 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.

    COPAL UA-512 DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209115556·KIT, PABC 8-PACK (vac) - CUSTOM

    Gemini Sterilization Wrap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VYGON LEADER-FLEX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    APEX FLEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·October 4, 2010

    11.0MM TI HELICAL BLADE 100MM

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·November 30, 2012