ENSEAL G2 CURVED JAW 35CM NSLG2C35

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2020-03-31 for ENSEAL G2 CURVED JAW 35CM NSLG2C35 manufactured by Ethicon Endo-surgery, Llc..

MAUDE Entry Details

Report Number3005075853-2020-01888
MDR Report Key9908302
Report SourceDISTRIBUTOR,FOREIGN
Date Received2020-03-31
Date of Report2020-03-09
Date of Event2020-01-24
Date Mfgr Received2020-03-09
Device Manufacturer Date2019-07-30
Date Added to Maude2020-03-31
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 ContactMS. KARA DITTY-BOVARD
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Country*
Manufacturer Postal00969
Manufacturer Phone6107428552
Manufacturer G1ETHICON ENDO-SURGERY, LLC.
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Country*
Manufacturer Postal Code00969
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameENSEAL G2 CURVED JAW 35CM
Generic NameELECTROSURGICAL CUTTING & COAGULATION & ACCESSORIES
Product CodeGEI
Date Received2020-03-31
Model NumberNSLG2C35
Catalog NumberNSLG2C35
Lot NumberT94089
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, LLC.
Manufacturer Address475 CALLE C GUAYNABO 00969 * 00969


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-31

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