BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    JLK-CTP

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Medos International Sàrl·10886705028290·Obturator for use with 2.8mm sheath compatible ...

    TOTAL MANDIBULAR SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036062842·

    SHINEBALL PVC MANUAL RESUSCIATOR, ENT-1001, ENT-1003, ENT-1005, SHINEBALL SILICONE MANUAL RESUSCIATOR, ENT-1022,

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Flexible Video-Uretero-Choledochoscope System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ADVIA CENTAUR TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·November 21, 2008

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 23, 2013

    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