BEUDAMED
    14 results · 27ms · Sources: EU EUDAMED, US FDA

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    NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Unclassified ·Unknown

    Crosperio RX PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD), MODEL SV-S23BL35VS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 4, 2019

    MEDTRONIC.SIGMA

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·February 9, 2013

    TENOR

    FDA Adverse Event
    Other ·MEDIBO MEDICAL PRODUCTS NV·Product code FSA·December 2, 2010

    16" EAGLE STEAM STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·July 23, 2014

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 1, 2024

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 10, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 18, 2022

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 2, 2021

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 6, 2022