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

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    MANTARAY GUIDEWIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ArgenPMMA 98x20-C1

    FDA UDI
    ARGEN CORPORATION, THE·D818120881·Crown And Bridge, Temporary, Resin

    MODIFICATION TO PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNAPSE OBLIQUUS MIP/MPR/FUSION

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 21, 2024

    ASR XL TAP SLV ADAP 12/14+5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    HIP IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·September 26, 2014

    CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 11, 2011

    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

    LACRIFAST

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

    LACRIFAST

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code OKS·June 2, 2021