BEUDAMED
    10,000 results · 48ms · 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.

    *

    FDA Adverse Event
    Injury ·ERIE MEDICAL·Product code CAN·February 11, 2004

    Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663

    FDA Recall
    Terminated ·St. Jude Medical, Inc.·Product code MHY·September 12, 2017

    Proclaim DRG Implantable Pulse Generator Model 3664

    FDA Recall
    Terminated ·St. Jude Medical, Inc.·Product code LGW·September 12, 2017

    Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Implantable Pulse Generator Models 3660, 3661, 3662, 3663, 3665, 3667

    FDA Recall
    Terminated ·St. Jude Medical, Inc.·Product code LGW·September 12, 2017

    PHILOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code DXY·November 2, 2005

    SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 15, 2015

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 4, 2016

    LEXOS DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO.·Product code LWS·September 2, 2009

    ACTROS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.,·Product code DTB·September 19, 2005

    QUADRA ASSURA (DDQP+)

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·July 18, 2018

    PROCLAIM 5 ELITE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 6, 2018

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NIK·January 12, 2018

    UNIFY CRT-D

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NIK·December 18, 2017

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 9, 2016

    ILESTO 7 DR-T DF-1

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·May 14, 2020

    FORTIFY ASSURA DR ICD, US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·December 6, 2016

    PROCLAIM 7 ELITE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 7, 2018

    FORTIFY DR, U1.6 DF1 ID

    FDA Adverse Event
    Malfunction ·ABBOTT·Product code LWS·August 30, 2019

    UNIFY QUADRA CRT-D, OUS MODEL, DF4COMP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NIK·November 28, 2016

    FORTIFY ST DR, U1.6 SJ4 ID

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·December 6, 2016