BEUDAMED
    10 results · 35ms · Sources: EU EUDAMED, US FDA

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    MVP (MULTI-VENDOR PROTOCOL CONVERTOR)

    FDA 510(k)
    FDA Class 1 ·Radiology

    3M™ Unitek™

    FDA UDI
    3M COMPANY·30605861027770·3M™ Unitek™ Stainless Steel Second Primary Mola...

    UMBICUT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SAS FLUALERT A&B, SAS INFLUENZA A TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MPACT FLAT PE HC LINER 40/G

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 15, 2021

    LINER: MPACT FLAT PE HC LINER 40/G

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 12, 2021

    EVOLVE

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH, INC.·Product code IKY·May 2, 2014

    MARQUIS SERIES STOPCOCKS

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DTL·October 25, 2010

    MULTIRALL 200

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·November 13, 2012

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009