BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    AMSafe NeuFlo Needleless Connector

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ambIT* Cassette - Filterless, Male Luer

    FDA UDI
    Avanos Medical, Inc.·00193494001094·ambIT* Cassette - Filterless, Male Luer

    ambIT

    FDA UDI
    SUMMIT MEDICAL PRODUCTS, INC.·00857595005091·Cassette - Filterless, Male Luer

    FILMARRAY RP PANEL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OPTILUX CURING LIGHTS

    FDA 510(k)
    FDA Class 2 ·Dental

    BD RAPID DETECTION OF SARS-COV-2 VERITOR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·October 27, 2020

    FREESTYLE FREEDOM LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·October 31, 2008

    LAMITRODE TRIPOLE 16 LEAD, 60 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 16, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

    ambIT Ambulatory Infusion Pump Cassette; Filterless, Male, Sterile, Vol. 2.3ml, REF 220267, Sorenson Medical, Inc., West Jordan, Utah.

    FDA Recall
    Terminated ·Sorenson Medical, Inc.·Product code FRN·October 10, 2006