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.

    OREIA-Q-DIG

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MDI GLIADIN A TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·May 9, 2014

    IDRT-TS (INTL) SINGLE 4X5

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code MGR·October 19, 2012

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·May 28, 2015