35 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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A8, A9 Anesthesia System
FDA 510(k)
FDA Class 2
·Anesthesiology
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958002441·Medilas D LiteBeam+ Diode Laser, 1470 nm, D-Plug
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3
MODULAR ROTATING HINGE KNEE TIBIAL ROTATING COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Brainsway Deep TMS System
FDA 510(k)
FDA Class 2
·Neurology
ENDURANT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
TALENT AAA STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
GORE VIABAHN ENDOPROSTHESIS - 3
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code PFV·August 5, 2019
ENDURANT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
TALENT AAA STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
ENDURANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·October 24, 2019
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
ENDURANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·June 13, 2019
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·October 24, 2019
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 2, 2013
GORE VIABAHN ENDOPROSTHESIS - 3
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code PFV·October 25, 2019
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD
FDA Adverse Event
Injury
·COVIDIEN·Product code FGE·April 26, 2019
PROTEGE RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·COVIDIEN·Product code NIM·April 26, 2019