BEUDAMED
    8 results · 22ms · 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.

    YellowStar

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

    Glenosphere trial Ø42

    FDA UDI
    FOURNITURES HOSPITALIERES INDUSTRIE·03661489610943·

    iMap 3D Mapping & Navigation System (iMap System)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEWPORT E500 WAVE VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    E500 VENTILATOR SYSTEM

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·July 11, 2016

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 19, 2014

    TOTAL ASR FEM IMP SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 23, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·August 2, 2013