TRUCLEAR 7210165

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-09-30 for TRUCLEAR 7210165 manufactured by Smith & Nephew.

MAUDE Entry Details

Report Number1643264-2019-20020
MDR Report Key9135984
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-09-30
Date of Report2019-09-30
Date of Event2019-09-01
Date Mfgr Received2019-09-05
Date Added to Maude2019-09-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactLISA HERNANDEZ
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CT 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone2034925563
Manufacturer G1SMITH & NEPHEW
Manufacturer Street150 MINUTEMAN RD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRUCLEAR
Generic NameINSUFFLATOR, HYSTEROSCOPIC
Product CodeHIG
Date Received2019-09-30
Returned To Mfg2019-09-19
Model Number7210165
Catalog Number7210165
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW
Manufacturer Address150 MINUTEMAN RD ANDOVER MA 01810 US 01810


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.