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

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    MS DISPOSABLE RIGID DOPPLER PROBE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515093058·Ortho Mallet, solid head, 1 lb, 7"

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M9302270·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515237759·Ortho Mallet, solid head, 1 lb, 7"

    T-Line Hernia Mesh

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SUTURTEK FASTCLOSE SUTURING DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HUMERAL GUIDE WIRE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HXI·November 23, 2010

    THORACIC GRASPER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code GEI·January 25, 2013

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FPA·July 11, 2014

    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