BEUDAMED
    6 results · 22ms · 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.

    MODIFIED SITE DISPOSABLE DIAPHRAGM CASSETTE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ELISA TUBE PROLACTIN TEST KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CATHETER CHOLANGIOGRAPHY

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

    LARGE NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 22, 2013

    SPRINT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    BIPOLAR VENTRICULAR ENDOCARDIAL LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·July 10, 2014