DRAGONFLY IMAGING CATHETER 13751-02 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2012-10-11 for DRAGONFLY IMAGING CATHETER 13751-02 NA manufactured by St. Jude Medical.

Event Text Entries

[2919326] During a procedure to analyze plaque utilizing oct imaging pt experienced ventricular fibrillation. The pt was reported to be stable.
Patient Sequence No: 1, Text Type: D, B5


[10382692] The device history record was reviewed and the device was manufactured in accordance to sjm specs.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004672267-2012-00007
MDR Report Key2793831
Report Source05,06,07
Date Received2012-10-11
Date of Report2012-09-11
Date of Event2012-09-10
Date Mfgr Received2012-09-11
Device Manufacturer Date2011-09-30
Date Added to Maude2012-10-18
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 FDA0
Event Location0
Manufacturer ContactANN GRAVES
Manufacturer StreetONE TECHNOLOGY PARK DRIVE
Manufacturer CityWESTFORD MA 01886
Manufacturer CountryUS
Manufacturer Postal01886
Manufacturer Phone9786921408
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDRAGONFLY IMAGING CATHETER
Generic NameINTERVASCULAR IMAGING CATHETER
Product CodeNQQ
Date Received2012-10-11
Model Number13751-02
Catalog NumberNA
Lot NumberDF-11-609
Device Expiration Date2013-09-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL
Manufacturer AddressWESTFORD MA US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2012-10-11

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