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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    FUKUDA DENSHI DYNASCOPE, MODEL DS-5800NX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741140396·Catheter Placement Kit

    TruLock

    FDA UDI
    Rmo, Inc.·00885797658289·TRULOCK Light Activated Adhesive Kit (4ea Syrin...

    Disposable Leadset,5 lead,24" snap,AAMI

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904086750·

    KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RADIOCAMERAS EXTRACRANIAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code FSA·March 12, 2013

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO·Product code BTR·February 16, 2011

    DIMENSION CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LTJ·February 19, 2008

    ENTERPRISE 5000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·August 1, 2023

    ENTERPRISE 5000

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB·Product code FNL·October 2, 2020

    ENTERPRISE 8000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·October 15, 2024

    ENTERPRISE 8000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·January 17, 2024

    ENTERPRISE 8000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·October 8, 2025

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·November 17, 2021