BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    SLIDEWIRETM(TRADEMARK PENDING)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABSOLUTE BI-POLAR SHOULDER SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304212459·

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664005689·FOR MEN CASUAL 30-40 MM HG KNEE HIGH CLOSED TOE...

    ELECSYS PTH CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    14F X 24CM ASH SPLIT-CATH,14F X 28CM ASH SPLIT-CATH, 14F X 32CM ASH SPLIT-CATH, 14FX36CM ASH SPLIT-CATH, 14F X 40CM ASH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ASCENSIA DEX2

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·May 22, 2006

    AUTODISC 100 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·August 7, 2006

    AUTODISC 50 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·January 29, 2008

    ASCENSIA BREEZE

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·May 5, 2006

    ASCENSIA BREEZE

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·June 12, 2006

    ASCENSIA BREEZE (TH)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·January 31, 2007

    BREEZE2

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·July 17, 2009

    AUTODISC 50 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 27, 2006

    AUTODISC 50 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·July 10, 2006

    ASCENSIA BREEZE (US)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 26, 2008

    ASCENSIA BREEZE (US)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code CGA·February 28, 2007

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·October 18, 2010

    VILEX

    FDA Adverse Event
    Malfunction ·VILEX, INC.·Product code JDW·June 4, 2012

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·May 9, 2013

    MBT CEM KEEL TIB TRAY SZ2.5

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code NJL·May 20, 2011