BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    CO2 ARTHROFLATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668106457·BISHOP-HARMON FORCEPS SERRATED

    ZAVATION

    FDA UDI
    Zavation LLC·00842166117259·Polyaxial Screw 3.5mm x 50mm

    AMBU BLUE SENSOR NEO AND NEO X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FTRD System Set

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PROTECTA XT CRT-D

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LWS·February 9, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 10, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2014