BEUDAMED
    49 results · 34ms · Sources: EU EUDAMED, US FDA

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    TRANSPORT CULTURE MEDIUM DEVICE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    WeightRight®

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734020616·Tungsten-Filled Maloney Esophageal Dilator, 46 ...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450264119·

    ULTIMA TENS XL-A1

    FDA 510(k)
    FDA Class 2 ·Neurology

    IMC SURGICAL FACE MASK

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

    COMFORT TOUCH INSUIN PEN NEEDLES

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA TECHNOLOGY CO., LTD.·Product code FMI·May 21, 2021

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 20, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 26, 2014

    CARELINK

    FDA Adverse Event
    Malfunction ·PLEXUS MANUFACTURING SDN. BHD.·Product code NVZ·June 11, 2011

    ARTERIAL PRESSURE MONITORING TRAY

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQO·December 3, 2024

    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

    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