RESECTRTM TISSUE RESECTION DEVICE M0065907051 74088

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-10 for RESECTRTM TISSUE RESECTION DEVICE M0065907051 74088 manufactured by Biomerics Llc.

MAUDE Entry Details

Report Number3005099803-2020-00741
MDR Report Key9811008
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-10
Date of Report2020-03-10
Date of Event2019-11-06
Date Mfgr Received2020-02-28
Device Manufacturer Date2017-11-08
Date Added to Maude2020-03-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1BIOMERICS LLC
Manufacturer Street6030 WEST HAROLD GATTY DRIVE
Manufacturer CitySALT LAKE CITY UT 84116
Manufacturer CountryUS
Manufacturer Postal Code84116
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRESECTRTM TISSUE RESECTION DEVICE
Generic NameHYSTEROSCOPE ACCESSORIES
Product CodeNWW
Date Received2020-03-10
Model NumberM0065907051
Catalog Number74088
Lot Number0009441380
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERICS LLC
Manufacturer Address6030 WEST HAROLD GATTY DRIVE SALT LAKE CITY UT 84116 US 84116


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-10

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