BEUDAMED
    24 results · 23ms · Sources: EU EUDAMED, US FDA

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    CAM Titanium Blanks

    FDA 510(k)
    FDA Class 2 ·Dental

    UC-CARE NAVIGO SYTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    KII 5 X 100 FIOS Z-THR

    FDA Adverse Event
    Injury ·APPLIED MEDICAL·Product code GCJ·April 11, 2012

    TRIFECTA VALVE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (CS-WOODRIDGE)·Product code LWR·July 7, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 10, 2013

    MEDEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FPA·August 8, 2008

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·April 18, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 2, 2020

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 18, 2021

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·April 21, 2021

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 21, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·January 25, 2024

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·January 29, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 12, 2020

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·March 12, 2020

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·December 8, 2022

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 31, 2022

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·October 10, 2019

    ADVANCED PATELLA 35MM 3 PEG IMPLANT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 9, 2024