BEUDAMED
    6 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 ×

    MODEL GT1ST CRYOSURGICAL INSTRUMENT

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

    BRIGHTWAY BRAND COLORED POWDER FREE NITRILE EXAMINATION GLOVES (ORANGE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HD-IVUS ULTRASOUND IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOTAK DSP

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·January 18, 2013

    SENSIA S

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NVZ·December 13, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 9, 2014