BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    PUNCTUAL OCCLUDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    DIAZYME LDL-CHOLESTEROL REAGENT, CALIBRATOR AND CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTS

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

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·February 21, 2013

    PERFORMANCE PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code INK·December 30, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 1, 2014

    DA-400CIII

    FDA Adverse Event
    Injury ·NAKANISHI INC. (NSK)·Product code EGS·May 26, 2015

    Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·July 1, 2015