BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    MODEL 250 LIQUID CHROMOTAGRAPHY PUMP

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RESPIGRAPH-RESPISOMNOGRAPH-RESPICENTRAL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WUERZBURG TITANIUM MINI BONE PLATES & BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Dental

    BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QJR·April 9, 2021

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 19, 2014

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 20, 2010

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 4, 2012

    Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)

    FDA Enforcement
    Class II ·Ongoing·Medtronic Inc.·November 29, 2017

    Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code FPA·September 10, 2017