BEUDAMED
    8 results · 27ms · 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.

    ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS311

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972086·posteriors; shade B4; size S; upper jaw

    Matira™ Anterior Cervical System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INFINITAS MINI-IMPLANT SYSTEM/GUIDANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 21, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 27, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 31, 2014

    Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific instruments to the 3.5 mm Low Profile Pelvic System Retractor Set.

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·August 26, 2015