33 results
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46ms
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Sources: EU EUDAMED, US FDA
QT Imaging, Inc.
FDA registration
QT Imaging, Inc.·2 products·🇺🇸 United States
QT Scanner 2000
FDA UDI
Qt Imaging, Inc.·00852619008003·The QT Scanner 2000 Model A is an automated and...
TRANSDUCER, ULTRASONIC, DIAGNOSTIC
FDA Adverse Event
Injury
·QT IMAGING, INC.·Product code ITX·September 29, 2025
QT SCANNER 2000 MODEL A
FDA Adverse Event
Injury
·QT IMAGING HOLDINGS, INC.·Product code IYO·October 30, 2025
MedNet EC-REP GmbH
Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices
OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·TRIVASCULAR, INC.·Product code MIH·June 26, 2014
ACCULIS ACCU2I PMTA APPLICATOR
FDA Adverse Event
Malfunction
·MICROSULIS MEDICAL LTD.·Product code NEY·April 1, 2011
OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·TRIVASCULAR, INC.·Product code MIH·December 31, 2014
SPACEOAR SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OVB·December 21, 2023
OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·TRIVASCULAR, INC.·Product code MIH·January 17, 2015
OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·TRIVASCULAR, INC.·Product code MIH·June 26, 2014
OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·TRIVASCULAR, INC.·Product code MIH·March 16, 2015
MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·July 27, 2023
CERTUS 140 2.45 GHZ ABLATION SYSTEM
FDA Adverse Event
Injury
·Product code GEI·April 7, 2015
BARRICAID
FDA Adverse Event
Malfunction
·INTRINSIC THERAPEUTICS·Product code QES·August 11, 2020
MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·February 4, 2019
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 18, 2015
SPACEOAR VUE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OVB·December 12, 2022
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 18, 2015
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 18, 2015