BEUDAMED
    10,000 results · 201ms · Sources: EU EUDAMED, US FDA

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    MAS PAR TDM Liquid Assayed Therapeutic Drug Control

    FDA UDI
    Microgenics Corporation·00884883011694·

    ARROW-TREROTOLA PTD CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT:

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·January 17, 2019

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·January 9, 2019

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·October 5, 2018

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·February 14, 2018

    PERC. THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DXE·February 6, 2009

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·August 6, 2020

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·August 16, 2019

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT: 7

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·November 8, 2020

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DXE·August 21, 2020

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·February 20, 2018

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET: 5

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DXE·February 23, 2021

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET: 5

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DXE·January 22, 2021

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·July 23, 2019

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT: 7

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·June 14, 2021

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·October 19, 2018

    ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DXE·September 4, 2020