BEUDAMED
    7 results · 21ms · 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 ×

    LOGIQ E10

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506061882·Darrach-type Elevator , Overall Length: 10", Bl...

    ENK FIBEROPTIC ATOMIZER SET

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    TWIN STAR EXTREMITY COMPARTMENT SYNDROME MONITOR AND FLUID COLLECTION CATHETER SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code IZL·September 1, 2011

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 4, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 17, 2013