BEUDAMED
    6 results · 18ms · 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.

    HEMOSPENSER CARTRIDGE CAT. NO. 523500-

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SPECTRANETICS VISISHEATH DILATOR SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEIVS TRACHEOTOMY RETRACTOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 18, 2014

    *

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code NRA·October 5, 2012

    VIRTUOSO II VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2010