5MM ELASTIC STAYS 3311-1G

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-01-15 for 5MM ELASTIC STAYS 3311-1G manufactured by Coopersurgical, Inc..

MAUDE Entry Details

Report Number1216677-2019-00326
MDR Report Key9591222
Report SourceCONSUMER
Date Received2020-01-15
Date of Report2020-01-15
Date of Event2019-12-13
Date Mfgr Received2019-12-23
Device Manufacturer Date2018-12-18
Date Added to Maude2020-01-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. PETER NIZIOLEK
Manufacturer Street50 CORPORATE DRIVE -
Manufacturer CityTRUMBULL CT 06611
Manufacturer CountryUS
Manufacturer Postal06611
Manufacturer Phone2036015200
Manufacturer G1COOPERSURGICAL, INC.
Manufacturer Street75 CORPORATE DRIVE
Manufacturer CityTRUMBULL CT 06611
Manufacturer CountryUS
Manufacturer Postal Code06611
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name5MM ELASTIC STAYS
Generic Name5MM ELASTIC STAYS 50/CS
Product CodeGAD
Date Received2020-01-15
Model Number3311-1G
Catalog Number3311-1G
Lot Number260715
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOOPERSURGICAL, INC.
Manufacturer Address95 CORPORATE DRIVE TRUMBULL CT 06611 US 06611


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-15

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