TUR IRRIGATION SET VMC4005

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 2019-09-13 for TUR IRRIGATION SET VMC4005 manufactured by Baxter Healthcare - Tunisia.

MAUDE Entry Details

Report Number1416980-2019-05027
MDR Report Key9039395
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-09-13
Date of Report2019-10-15
Date Mfgr Received2019-09-24
Device Manufacturer Date2018-11-28
Date Added to Maude2019-09-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHARMACIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - TUNISIA
Manufacturer StreetROUTE DE CHEBBAOU 2021OUED E
Manufacturer CityTUNIS
Manufacturer CountryTS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTUR IRRIGATION SET
Generic NameSYSTEM, IRRIGATION, UROLOGICAL
Product CodeLJH
Date Received2019-09-13
Returned To Mfg2019-09-11
Model NumberNA
Catalog NumberVMC4005
Lot Number18K10T431N
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - TUNISIA
Manufacturer AddressTUNIS


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-13

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