BEUDAMED
    56 results · 25ms · Sources: EU EUDAMED, US FDA

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    CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODCER 65CM CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER 80CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694002707·Orbital Floor Plate, Large

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036031428·

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319719923·Tissue Forceps 6" (15cm), 4x5 teeth

    VISIUSmatrix

    FDA UDI
    IMRIS Imaging, Inc.·00857534006677·Applications Platform 4.0 INTL – INT KIT

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197029278·Fine Iris Eye Scissor 12.0 c...

    IFS PROFILE PLATES, SCREWS, AND WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECSYS CA 125 II CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 20, 2024

    GIRAFFE OMNIBED

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE, LLC·Product code FMZ·May 15, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·August 15, 2008

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 5, 2017