MERSILENE POLYESTER FIBER SUTURE GEEH7350H

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2019-06-13 for MERSILENE POLYESTER FIBER SUTURE GEEH7350H manufactured by Ethicon Inc..

MAUDE Entry Details

Report Number2210968-2019-82734
MDR Report Key8698256
Report SourceFOREIGN
Date Received2019-06-13
Date of Report2019-05-17
Date Mfgr Received2019-06-17
Device Manufacturer Date2018-11-13
Date Added to Maude2019-06-13
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 ContactDARLENE KYLE
Manufacturer StreetP.O. BOX 151, ROUTE 22 WEST
Manufacturer CitySOMERVILLE NJ 088760151
Manufacturer CountryUS
Manufacturer Postal088760151
Manufacturer Phone9082182792
Manufacturer G1ETHICON INC.-SAN LORENZO PR
Manufacturer StreetROAD 183, KM. 8.3
Manufacturer CitySAN LORENZO PR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMERSILENE POLYESTER FIBER SUTURE
Generic NameINSTRUMENT, SURGICAL, DISPOSABLE
Product CodeKDC
Date Received2019-06-13
Returned To Mfg2019-06-25
Catalog NumberGEEH7350H
Lot NumberMMH720
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerETHICON INC.
Manufacturer AddressP.O. BOX 151, ROUTE 22 WEST SOMERVILLE NJ 088760151 US 088760151


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-13

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