3,949 results
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32ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Front load bipolar electrode
FDA UDI
CHIRURGIE INNOVATION·03760263240052·(Fr26)
SYMPHONY
FDA Adverse Event
Injury
·SORIN CRM·Product code NVZ·December 5, 2014
PERMANENT PACEMAKER ELECTRODE
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code DTB·August 12, 2023
ENDURANT II STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·December 5, 2024
ENDURANT II STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·December 5, 2024
TIGER MOXA -YOUNG SHIN HEALTH
FDA Adverse Event
Malfunction
·YOUNG SHIN HEALTH, LLC·Product code MVV·January 14, 2010
SEA BAND
FDA Adverse Event
SEA-BAND, LTD.·Product code MVV·March 3, 2023
PIATREI MOTION SICKNESS BANDS
FDA Adverse Event
Injury
·UNK·Product code MVV·January 2, 2024
ANTI-NAUSEA WRISTBAND, RECHARGEABLE RELIEVE NAUSEA MOTION SICKNESS BANDS, RELIEV
FDA Adverse Event
Injury
·UNK·Product code MVV·December 9, 2022
ANTI-NAUSEA WRISTBAND
FDA Adverse Event
Malfunction
·UNKNOWN·Product code MVV·October 27, 2022
UNKNOWN KNEE INSTRUMENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·May 14, 2019
CUSTOM MONITORING KIT
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code DRS·May 15, 1998
CUSTOM MONITORING KIT
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code DRS·May 15, 1998
HAKIM VALVE INLINE UNIT (INTEGRAL CON)
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·November 30, 2017
EDWARDS SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code NPT·February 4, 2013
DRAINS OASIS SINGLE
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·September 19, 2022
DRAINS OASIS SINGLE
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·September 19, 2022
Psi Bands acupressure/acustimulation wrist bands in the following colors: Racer Black (UPC 859570001036), Daisy Chain (UPC 859570001029), Color Play (UPC 859570001043) and Cherry Blossom (UPC 859570001012).
FDA Recall
Terminated
·Psi Health Solutions·Product code MVV·April 26, 2007
Device, Acupressure
FDA classification
FDA Unclassified
·Device, Acupressure
M.V. S.R.L.
FDA registration
M.V. S.R.L.·2 products·🇮🇹 Italy