BEUDAMED
    7 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.

    SAFETY VEST/SHOULDER STRAP VEST/ECONOMY SAFETY VEST

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VIVA combo RF System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110

    FDA 510(k)
    FDA Class 2 ·General Hospital

    G7 LINER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·April 3, 2018

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2014

    PLUM LC OL CNVRTBL P

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 20, 2010

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·February 13, 2013