BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    AMSINO I.V. START KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100751·3-piece, monofocal, hydrophobic, acrylic, intra...

    VBMAX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AT HOME DRUG TEST, MODEL 9078 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    TERUFLEX BLOOD BAG SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION/TERUMO BCT·Product code KSR·April 10, 2013

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011

    Z NAIL CMF 10.5 X 95 LAG SCR

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·August 12, 2021

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012