F8 DIALYZER FINISHED ASSY (CASE) 0500164A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-01-16 for F8 DIALYZER FINISHED ASSY (CASE) 0500164A manufactured by Ogden Manufacturing Plant.

MAUDE Entry Details

Report Number1713747-2020-00017
MDR Report Key9596660
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-01-16
Date of Report2020-01-28
Date of Event2019-12-20
Date Mfgr Received2020-01-27
Device Manufacturer Date2017-02-28
Date Added to Maude2020-01-16
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 ContactMATTHEW AMARAL
Manufacturer Street920 WINTER ST
Manufacturer CityWALTHAM MA 02451
Manufacturer CountryUS
Manufacturer Postal02451
Manufacturer Phone7816999758
Manufacturer G1OGDEN MANUFACTURING PLANT
Manufacturer StreetDIRECTOR, SITE QUALITY 475 WEST 13TH STREET
Manufacturer CityOGDEN UT 84404
Manufacturer CountryUS
Manufacturer Postal Code84404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameF8 DIALYZER FINISHED ASSY (CASE)
Generic NameDIALYZER, CAPILLARY, HOLLOW FIBER
Product CodeFJI
Date Received2020-01-16
Model Number0500164A
Catalog Number0500164A
Lot Number17BU04023
Device Expiration Date2020-02-29
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeMO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOGDEN MANUFACTURING PLANT
Manufacturer AddressDIRECTOR, SITE QUALITY 475 WEST 13TH STREET OGDEN UT 84404 US 84404


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-16

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