108 results
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62ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ABLATIVE SOLUTIONS, INC.
FDA registration
ABLATIVE SOLUTIONS, INC.·1 product·🇺🇸 United States
Peregrine System Infusion Catheter
FDA UDI
ABLATIVE SOLUTIONS, INC.·00862468000318·Peregrine System Infusion Catheter, US
Peregrine System™ Infusion Catheter
FDA UDI
ABLATIVE SOLUTIONS, INC.·00862468000349·Peregrine System™ Infusion Catheter (4-7 mm), 5...
Peregrine System™ Infusion Catheter
FDA UDI
ABLATIVE SOLUTIONS, INC.·00862468000356·Peregrine System™ Infusion Catheter (3-4 mm), 5...
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·September 18, 2024
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·January 29, 2025
PENTARAY NAV
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code MTD·September 18, 2024
ACUSON ACUNAV 10F ULTRASOUND CATHETER
FDA Adverse Event
Injury
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code OBJ·December 1, 2017
OCTARAY MAPPING CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code MTD·May 6, 2025
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·April 3, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·December 31, 2023
ACUSON ACUNAV 10F-64 ULTRASOUND CATHETER
FDA Adverse Event
Injury
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code OBJ·December 5, 2017
PREFACE® GUIDING SHEATH WITH MULTIPURPOSE CURVE
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC.·Product code DYB·July 31, 2019
PENTARAY NAV
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code MTD·September 11, 2025
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·December 31, 2023
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - SMALL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·October 3, 2022
THERMOCOOL SMARTTOUCH
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·July 9, 2025
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - SMALL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·April 23, 2024
THERMOCOOL® SMART TOUCH® SF UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·December 11, 2024
VARIPULSE¿ BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code QZI·May 20, 2026