349 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NEOTRACT, INC.
FDA registration
NEOTRACT, INC.·2 products·🇺🇸 United States
UroLift® 2
FDA UDI
NEOTRACT, INC.·00814932020025·
UroLift® 2
FDA UDI
NEOTRACT, INC.·00814932020032·
UroLift® 2
FDA UDI
NEOTRACT, INC.·00814932020018·
UroLift
FDA UDI
NEOTRACT, INC.·00814932020001·
UroLift
FDA UDI
NEOTRACT, INC.·00814932020049·
UROLIFT
FDA Adverse Event
Malfunction
·NEOTRACT, INC.·Product code PEW·April 3, 2020
UROLIFT
FDA Adverse Event
Malfunction
·NEOTRACT, INC.·Product code PEW·March 29, 2022
NEOTRACT UROLIFT 2 SYSTEM
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·October 23, 2024
NEOTRACT UROLIFT 2 SYSTEM
FDA Adverse Event
Malfunction
·HUDSON RESPIRATORY CARE TECATE·Product code PEW·January 6, 2025
NEOTRACT UROLIFT SYSTEM UL400
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·June 28, 2019
NEOTRACT UROLIFT SYSTEM UL400
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·July 5, 2019
NEOTRACT UROLIFT SYSTEM
FDA Adverse Event
Malfunction
·HUDSON RESPIRATORY CARE TECATE·Product code PEW·April 23, 2025
NEOTRACT UROLIFT SYSTEM UL400
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·June 14, 2019
NEOTRACT UROLIFT SYSTEM
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·October 16, 2024
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
FDA Recall
Open, Classified
·Neotract Inc·Product code PEW·June 24, 2022
NEOTRACT UROLIFT SYSTEM
FDA Adverse Event
Injury
·HUDSON RESPIRATORY CARE TECATE·Product code PEW·March 12, 2025
UROLIFT BENIGN PROSTATIC HYPERPLASIA IMPLANT AND APPLICATOR
FDA Adverse Event
Injury
·TELEFLEX, COM, NEOTRACT / NEOTRACT, INC.·Product code PEW·July 14, 2025
NEOTRACT UROLIFT SYSTEM UL400
FDA Adverse Event
Injury
·NEOTRACT INC.·Product code PEW·December 21, 2016
NEOTRACT UROLIFT SYSTEM UL400
FDA Adverse Event
Injury
·NEOTRACT, INC.·Product code PEW·July 1, 2015