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.
[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
Report Number | 3009600098-2019-00010 |
MDR Report Key | 8546870 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-04-24 |
Date of Report | 2019-06-20 |
Date of Event | 2019-04-05 |
Date Mfgr Received | 2019-06-13 |
Device Manufacturer Date | 2016-08-22 |
Date Added to Maude | 2019-04-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | STEPHANIE O' SULLIVAN |
Manufacturer Street | 5050 NATHAN LANE NORTH |
Manufacturer City | PLYMOUTH MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 6517565400 |
Manufacturer G1 | ST. JUDE MEDICAL CATD |
Manufacturer Street | 4 ROBBINS DRIVE |
Manufacturer City | WESTFORD MA 01886 |
Manufacturer Country | US |
Manufacturer Postal Code | 01886 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | C8I ? OCT INTEGRATED SYSTEM |
Generic Name | SYSTEM, IMAGING, OPTICAL COHERENCE TOMOGRAPHY (OCT) |
Product Code | NQQ |
Date Received | 2019-04-24 |
Model Number | C408652 |
Lot Number | 5591593 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ST. JUDE MEDICAL CATD |
Manufacturer Address | 4 ROBBINS DRIVE WESTFORD MA 01886 US 01886 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-04-24 |