BEUDAMED
    7 results · 19ms · 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.

    SafeSept RF Transseptal Guidewire (SSRF132; SSRF132R; SSRF232; SSRF232R; SSRF135; SSRF135R; SSRF235; SSRF235R)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N Series Patient Monitors

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ProFlex CO2 Laser Fiber

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

    CLEARCORRECT SYSTEM

    FDA Adverse Event
    Injury ·CLEARCORRECT LLC·Product code NXC·September 30, 2020

    VITALITY 2 DR EL

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    TRAUMA TRANSTAR

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·August 10, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MPRI·Product code LWS·July 30, 2013