ASAHI APS HEMODIALYZER APS-10505 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-03-15 for ASAHI APS HEMODIALYZER APS-10505 NA manufactured by Nextron Medical.

Event Text Entries

[334367] Pt experienced chills at completion of hemodialysis therapy. Therapy was provided with an 18th use hemodialyzer.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number519310
MDR Report Key519310
Date Received2004-03-15
Date of Report2003-12-19
Date of Event2003-10-27
Date Facility Aware2003-10-27
Report Date2003-12-19
Date Reported to Mfgr2003-12-19
Date Added to Maude2004-04-08
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameASAHI APS HEMODIALYZER
Generic NameHEMODIALYZER
Product CodeFKP
Date Received2004-03-15
Model NumberAPS-10505
Catalog NumberNA
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key508373
ManufacturerNEXTRON MEDICAL
Manufacturer Address45 KULICK ROAD FAIRFIELD NJ 07004 US

Device Sequence Number: 2

Brand NameRENATRON
Generic NameREPROCESSING DEIVCE
Product CodeLIF
Date Received2004-03-15
Model NumberRS8330
Catalog NumberNA
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagN
Date RemovedA
Device Sequence No2
Device Event Key508376
ManufacturerMINNTECH CORP.
Manufacturer Address14605 28TH AVENUE NORTH MINNEAPOLIS MN 55447 US
Baseline Brand Name*
Baseline Generic NameHEMODIALZER
Baseline Model NoRS8330
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other 2004-03-15

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