18 results
·
33ms
·
Sources: EU EUDAMED, US FDA
SERVOMED COMPACT MONITOR 181/10105002
FDA 510(k)
FDA Class 2
·Cardiovascular
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780468967·Integra® Miltex® Friction Grip, Diamond Bur, Bu...
Continuum® Trilogy®
FDA UDI
Zimmer, Inc.·00889024153899·
Continuum® Trilogy®
FDA UDI
Zimmer, Inc.·00889024153882·
Continuum® Trilogy®
FDA UDI
Zimmer, Inc.·00889024153875·
EASY PULSE II OXYGEN CONSERVER
FDA 510(k)
FDA Class 2
·Anesthesiology
Citrated: K, KH, RTH, FFH
FDA 510(k)
FDA Class 2
·Hematology
PASSPORT 2 MONITOR
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code MHX·March 7, 2014
PULSE GEN MODEL 102
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·November 14, 2012
ACCURUS 800CS
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 3, 2010
NI
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GWM·November 21, 2018
NI
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GWM·November 21, 2018
IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code ONU·May 22, 2019
ZOLL QUATTRO EU CATHETER
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION·Product code NCX·September 12, 2018
NI
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GWM·February 27, 2019
NI
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GWM·February 27, 2019
PIPELINE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 29, 2020
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 29, 2020