NXSTAGE SYSTEM ONE SAK-403

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-08-29 for NXSTAGE SYSTEM ONE SAK-403 manufactured by Nxstage Medical, Inc..

MAUDE Entry Details

Report Number3003464075-2019-00042
MDR Report Key8945647
Report SourceCONSUMER
Date Received2019-08-29
Date of Report2019-08-29
Date of Event2019-08-16
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2019-08-19
Device Manufacturer Date2018-10-24
Date Added to Maude2019-08-29
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. PAULA ROGALSKI
Manufacturer StreetNXSTAGE MEDICAL, INC 350 MERRIMACK STREET
Manufacturer CityLAWRENCE MA 01843
Manufacturer CountryUS
Manufacturer Postal01843
Manufacturer Phone9784505276
Manufacturer G1MEDIMEXICO S. DE R. L. DE C. V
Manufacturer StreetAV. VALLE IMPERIAL NO. 10523 PARQUE INDUSTRIAL VALLE SUR
Manufacturer CityTIJUANA 22180
Manufacturer CountryMX
Manufacturer Postal Code22180
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNXSTAGE SYSTEM ONE
Generic NameHIGH PERMEABILITY HEMODIALYSIS SYSTEM
Product CodeFKR
Date Received2019-08-29
Model NumberSAK-403
Catalog NumberSAK-403
Lot Number81079205
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNXSTAGE MEDICAL, INC.
Manufacturer Address350 MERRIMACK STREET LAWRENCE MA 01843 US 01843


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-08-29

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