RENALIN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2005-01-07 for RENALIN manufactured by Minntech Corp..

Event Text Entries

[375574] Facility reports a tech had gotten renalin splashed in their eye while in the process of testing a dialyzer for the presence of renalin. Tech went to er, was treated and released the same day. Tech doing fine with no ill effects reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2150060-2005-00001
MDR Report Key565659
Report Source05,06
Date Received2005-01-07
Date of Report2005-01-07
Date of Event2004-12-09
Date Facility Aware2004-12-09
Report Date2005-01-07
Date Mfgr Received2004-12-09
Date Added to Maude2005-01-18
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 Location0
Manufacturer Street14605 28TH AVENUE NORTH
Manufacturer CityMINNEAPOLIS MN 55447
Manufacturer CountryUS
Manufacturer Postal55447
Manufacturer Phone7635533300
Manufacturer G1MINNTECH CORPORATION
Manufacturer Street14605 28TH AVENUE NORTH
Manufacturer CityMINNEAPOLIS MN 55447
Manufacturer CountryUS
Manufacturer Postal Code55447
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRENALIN
Generic NameCOLD STERILANT
Product CodeLIF
Date Received2005-01-07
Model NumberNA
Catalog NumberNA
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key555448
ManufacturerMINNTECH CORP.
Manufacturer Address14605 28TH AVE. NORTH MINNEAPOLIS MN 55447 US


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2005-01-07

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