BEUDAMED
    115 results · 24ms · 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 ×

    MagVita TMS Therapy w/MagPro R20

    FDA 510(k)
    FDA Class 2 ·Neurology

    SHARPS AWAY DISPOSABLE CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNERGY ODM

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD SYRINGE 30ML LL BNS

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·October 27, 2025

    D.A.S.H. DOMETIP DOUBLE LUMEN SPHINCTEROTOME

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code KNS·July 19, 2021

    UTS PRECURVED ULTRA TAPER SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·April 29, 2021

    TRI-TOME PC TRIPLE LUMEN SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNS·May 12, 2022

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 17, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·July 20, 2011

    TRUETRACK SMART SYSTEM

    FDA Adverse Event
    Malfunction ·HOEM DIAGNOSTICS INC.·Product code NBW·September 19, 2008

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (LOW PROFILE)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 30, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·April 3, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 26, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·September 26, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 4, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 9, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 3, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·October 12, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 7, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 11, 2020