10 results
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66ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR
FDA 510(k)
FDA Unclassified
·Unknown
SENSE TECHNOLOGY, INC.
FDA registration
SENSE TECHNOLOGY, INC.·1 product·🇺🇸 United States
PulStar
FDA UDI
Sense Technology, Inc.·00855341008006·The PulStar Spine Mobilization Device is intend...
SENECA SENSE TECHNOLOGIES INC
FDA registration
SENECA SENSE TECHNOLOGIES INC·1 product·🇨🇦 Canada
THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·November 27, 2014
THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·November 27, 2014
THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·November 27, 2014
THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·November 27, 2014
NYLON SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAR·December 13, 2021
LASSO¿ ELECTROPHYSIOLOGY CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DRF·October 12, 2022