ASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER 20301

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2009-12-18 for ASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER 20301 manufactured by Minntech Corp..

Event Text Entries

[1313673] The customer alleged fluid emitted from the pressure relief valve. Asp technical rep commented that the air valve was opening when it should be closed. There should not be any fluid in the line. Subsequently, the customer stated the unit leaked a small amount cidex opa solution onto the floor. No injuries or adverse effects were involved. The customer cleaned the skinner valve then reseated it to resolve the issue. The unit is in full operation.
Patient Sequence No: 1, Text Type: D, B5


[8510970] Capital equipment evaluated at the customer site. The customer cleaned and reseated the skinner valve to resolve the issue. The customer repaired the unit.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2150060-2009-00178
MDR Report Key1576995
Report Source05
Date Received2009-12-18
Date of Report2009-11-24
Date of Event2009-11-24
Date Mfgr Received2009-11-24
Date Added to Maude2010-03-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactGINNY STAMBERGER
Manufacturer Street33 TECHNOLOGY DR.
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9497893837
Manufacturer G1MINNTECH CORP.
Manufacturer Street14605 28TH AVE. NORTH
Manufacturer CityMINNEAPOLIS MN 55447
Manufacturer CountryUS
Manufacturer Postal Code55447
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER
Generic NameAER EQUIPMENT
Product CodeNVE
Date Received2009-12-18
Model NumberNA
Catalog Number20301
Lot NumberNA
ID NumberPART #: NA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMINNTECH CORP.
Manufacturer AddressMINNEAPOLIS MN 55447 US 55447


Patients

Patient NumberTreatmentOutcomeDate
10 2009-12-18

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