C8I ? OCT INTEGRATED SYSTEM C408652

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-04-24 for C8I ? OCT INTEGRATED SYSTEM C408652 manufactured by St. Jude Medical Catd.

Event Text Entries

[143033438] The results/method and conclusion codes along with investigation results will be provided in the final report.
Patient Sequence No: 1, Text Type: N, H10


[143033439] The procedure was postponed due to a connection issue that occurred after a catheter was disconnected without using the eject button. Another catheter was used but the issue persisted. The issue was isolated to the system. There were no adverse patient consequences.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009600098-2019-00010
MDR Report Key8546870
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-24
Date of Report2019-06-20
Date of Event2019-04-05
Date Mfgr Received2019-06-13
Device Manufacturer Date2016-08-22
Date Added to Maude2019-04-24
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 ContactSTEPHANIE O' SULLIVAN
Manufacturer Street5050 NATHAN LANE NORTH
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1ST. JUDE MEDICAL CATD
Manufacturer Street4 ROBBINS DRIVE
Manufacturer CityWESTFORD MA 01886
Manufacturer CountryUS
Manufacturer Postal Code01886
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameC8I ? OCT INTEGRATED SYSTEM
Generic NameSYSTEM, IMAGING, OPTICAL COHERENCE TOMOGRAPHY (OCT)
Product CodeNQQ
Date Received2019-04-24
Model NumberC408652
Lot Number5591593
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL CATD
Manufacturer Address4 ROBBINS DRIVE WESTFORD MA 01886 US 01886


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-04-24

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