MICRO-VOLUME EXTENSION SET 2N3350

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-09-19 for MICRO-VOLUME EXTENSION SET 2N3350 manufactured by Baxter Healthcare - Dominican Republic.

MAUDE Entry Details

Report Number1416980-2019-05135
MDR Report Key9088620
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-09-19
Date of Report2019-09-19
Date Mfgr Received2019-08-26
Date Added to Maude2019-09-19
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 Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - DOMINICAN REPUBLIC
Manufacturer StreetCARRETERA SANCHEZ KM 18.5 PARQUE INDUSTRIAL ITABO, PIISA
Manufacturer CityHAINA, SAN CRISTOBAL
Manufacturer CountryDR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMICRO-VOLUME EXTENSION SET
Generic NameFILTER, INFUSION LINE
Product CodeFPB
Date Received2019-09-19
Model NumberNA
Catalog Number2N3350
Lot NumberASKU
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - DOMINICAN REPUBLIC
Manufacturer AddressHAINA, SAN CRISTOBAL


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-19

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