BEUDAMED
    6 results · 20ms · 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 ×

    POP-N-LOK SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIGEL- MULTIFUNCTION ELECTRODE

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

    516YT DISPLAY DRIVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MULTILINK AUTOMIX

    FDA Adverse Event
    Other ·IVOCLAR VIVADENT, AG·Product code EMA·November 16, 2010

    5MM, 33CM PEEK MONOPOLAR HANDLE 33CM

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code KOG·January 4, 2013

    LINEAR 7.5 FR. 34CC IAB

    FDA Adverse Event
    Death ·DATASCOPE CORP·Product code DSP·July 2, 2014