BEUDAMED
    8 results · 18ms · 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.

    BETHEL PLUS MULTIPLE NAMES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDO-SCRUB®

    FDA UDI
    MEDTRONIC XOMED, INC.·20613994662037·SHEATH 1912042 5PK ES2 STRYKER 4MM/45DEG

    KINGYIELD WRIST BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KINETIC CANNULA

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

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·May 13, 2014

    IN TOUCH ZX (TEST STICKERS)

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 11, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·December 1, 2010

    Sure Vue Color Staph 150T, Sure Vue Color Staph 300T, Sure Vue SELECT Staph, biokit SELECT Staph 75T The product is used as an aid in the identification of Staphylococcus aureus from Culture

    FDA Enforcement
    Class II ·Terminated·Integrated Science Systems Inc·June 15, 2016