BEUDAMED
    6 results · 25ms · 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.

    BRONCHITRAC DF DUAL RESP/CATHETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    VASCON POLARIS GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHOCOLATE PTCA BOLLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PINN LNR CON +4 NEUT 32IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 27, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 15, 2012

    ABBOCATH-T 22G 1-1/4

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD., CONTRACT MFR FOR HOSPIRA INC.·Product code FOZ·August 17, 2010