IMAGER II ANGIOGRAPHIC CATHETER 38270

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 2020-03-17 for IMAGER II ANGIOGRAPHIC CATHETER 38270 manufactured by Boston Scientific Corporation.

Event Text Entries

[183920497] It was reported that a tip detachment occured. During a procedure involving an imager ii angiographic catheter, it was noted that the tip was detached. The physician snared the tip out successfully. The procedure was completed with the other device and no patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-03461
MDR Report Key9844576
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2020-03-11
Date Mfgr Received2020-03-11
Device Manufacturer Date2018-08-10
Date Added to Maude2020-03-17
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 ContactJAY JOHNSON
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone7634942574
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetUNIT 7 8 AND 9
Manufacturer CityANNACOTTY, LI
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMAGER II ANGIOGRAPHIC CATHETER
Generic NameCATHETER, INTRAVASCULAR, DIAGNOSTIC
Product CodeDQO
Date Received2020-03-17
Model Number38270
Catalog Number38270
Lot Number0000133737
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressTWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.