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.

    SOYEE ALUMINUM INTERSPACED X-RAY GRID

    FDA 510(k)
    FDA Class 1 ·Radiology

    CLYDESDALE PTC™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169191082·CAGE 4926445 CDALE PTC 22MM 6 DEG 14X45

    Clydesdale™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994972613·CAGE 2926445 CLYDESDALE 22 6 DEG 14X45

    DEGUBOND PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC·Product code LZG·January 14, 2013

    KAPPA 700 SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·December 14, 2010

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 10, 2014