3,949 results · 32ms · Sources: EU EUDAMED, 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