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

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    RSX 30HF

    FDA 510(k)
    FDA Class 1 ·Radiology

    Barco

    FDA UDI
    Barco NV·05415334001817·MDSC-8231 MNA

    Barco

    FDA UDI
    Barco NV·05415334001961·MDSC-8255 MNA NG

    Barco

    FDA UDI
    Barco NV·05415334004610·MDRC-2222 CK CT

    BARD ENDOTRACHEAL TUBE, CUFFED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM

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

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·December 16, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 12, 2014

    Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)

    FDA Enforcement
    Class II ·Terminated·Barco Inc.·November 11, 2015

    Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander The intended use of the linear accelerator is to deliver x-ray radiation for therapeutic treatment of cancer.

    FDA Enforcement
    Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 2, 2014