TERUMO CDI 500 BLOOD PARAMETER MONITOR 500AHCT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,07 report with the FDA on 2011-06-13 for TERUMO CDI 500 BLOOD PARAMETER MONITOR 500AHCT manufactured by Terumo Cardiovascular System Corp..

Event Text Entries

[2134960] During routine testing of the device at the service ctr, the service tech reported that the auxiliary board was out specification. Since the event occurred during routine testing, there was no pt involvement during this event.
Patient Sequence No: 1, Text Type: D, B5


[9274701] Eval in progress, but not yet concluded.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1828100-2011-01655
MDR Report Key2185943
Report Source00,07
Date Received2011-06-13
Date of Report2011-06-13
Date of Event2011-05-19
Date Mfgr Received2011-05-19
Date Added to Maude2011-09-02
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 FDA0
Event Location0
Manufacturer ContactREBECCA ANDERSEN
Manufacturer Street6200 JACKSON RD.
Manufacturer CityANN ARBOR MI 48103
Manufacturer CountryUS
Manufacturer Postal48103
Manufacturer Phone7346634145
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTERUMO CDI 500 BLOOD PARAMETER MONITOR
Generic NameON LINE BLOOD GAS MONITOR
Product CodeLCM
Date Received2011-06-13
Returned To Mfg2010-12-15
Model Number500AHCT
Catalog Number500AHCT
OperatorOTHER
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTERUMO CARDIOVASCULAR SYSTEM CORP.
Manufacturer AddressANN ARBOR MI 48103 US 48103


Patients

Patient NumberTreatmentOutcomeDate
10 2011-06-13

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