BEUDAMED
    9 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 ×

    IMMULITE 2000 AUTOMATED IMMUNOASSAY ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970227·anteriors; shade B3; mould UBM

    PERMOBIL SUPERIOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OPUS MAGNUM PI KNOTLESS FIXATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    TAXUS¿ LIBERTÉ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 20, 2013

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 25, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·July 31, 2014

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009