ENDOPATH*THORACIC TROCAR SLEEV TT012

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-12-17 for ENDOPATH*THORACIC TROCAR SLEEV TT012 manufactured by Ethicon Endo-surgery, Llc..

MAUDE Entry Details

Report Number3005075853-2019-24494
MDR Report Key9485054
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2019-12-17
Date of Report2019-11-27
Date of Event2019-11-01
Date Mfgr Received2019-11-27
Device Manufacturer Date2019-05-20
Date Added to Maude2019-12-17
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 ContactMS. KARA DITTY-BOVARD
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Postal00969
Manufacturer Phone6107428552
Manufacturer G1ETHICON ENDO-SURGERY, LLC.
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Postal Code00969
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameENDOPATH*THORACIC TROCAR SLEEV
Generic NameCANNULA, SURGICAL, GENERAL & PLASTIC SURGERY
Product CodeGEA
Date Received2019-12-17
Catalog NumberTT012
Lot NumberT40G1E
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 2019-12-17

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