BEUDAMED
    1,184 results · 29ms · Sources: EU EUDAMED, US FDA

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    LGO-Surgical Laser Fibers

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

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 2, 2021

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM DEXCOM SHARE SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·February 9, 2016

    CALL CORD,7700,SGL,NUR,1/4-2C,NO LGO,GRY

    FDA UDI
    Crest Healthcare Supply·B4847700GYGL0·CALL CORD,7700,SINGLE, NURSE, 1/4 PHONE JACK, 2...

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 30, 2019

    LABSCREEN SINGLE ANTIGEN CLASS I

    FDA Adverse Event
    Malfunction ·ONE LAMBDA INC.·Product code LGO·July 27, 2009

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 19, 2021

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 28, 2015

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·August 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·February 25, 2021

    ENDURANT II STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 27, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 27, 2019

    ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG

    FDA Adverse Event
    Injury ·COOK INC·Product code MIH·May 23, 2025

    GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·February 5, 2026

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 19, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 16, 2019

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·June 9, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·May 20, 2021

    CENTRIMAG MOTOR, OUS

    FDA Adverse Event
    Malfunction ·THORATEC SWITZERLAND GMBH·Product code KFM·April 19, 2021