TRANS-RAY 7FR. 34CC 0684-00-0513

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 2020-03-30 for TRANS-RAY 7FR. 34CC 0684-00-0513 manufactured by Datascope Corp. - Fairfield.

Event Text Entries

[185521330] Event site postal code - (b)(4). Complete event site name - (b)(4) mc. The device has not been returned to the manufacturer so we are unable to complete an evaluation. If provided we will send a supplemental report with our additional findings. Complaint record id#: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[185521331] It was reported during emergency percutaneous coronary intervention (pci), insertion of the intra-aortic balloon (iab), the guide wire did not insert into the iab catheter. The customer tried several times but failed. Another iab was used to start therapy. There was no reported injury to the patent.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2248146-2020-00177
MDR Report Key9897811
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-02-16
Date Mfgr Received2020-03-09
Device Manufacturer Date2019-06-05
Date Added to Maude2020-03-30
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 ContactMS. DOROTA WOLPIUK
Manufacturer Street15 LAW DRIVE
Manufacturer CityFAIRFIELD NJ 07004
Manufacturer CountryUS
Manufacturer Postal07004
Manufacturer G1DATASCOPE CORP. - FAIRFIELD
Manufacturer Street15 LAW DRIVE
Manufacturer CityFAIRFIELD NJ 07004
Manufacturer CountryUS
Manufacturer Postal Code07004
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANS-RAY 7FR. 34CC
Generic NameSYSTEM, BALLOON, INTRA-AORTIC AND CONTROL
Product CodeDSP
Date Received2020-03-30
Catalog Number0684-00-0513
Lot Number3000097974
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerDATASCOPE CORP. - FAIRFIELD
Manufacturer Address15 LAW DRIVE FAIRFIELD NJ 07004 US 07004


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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