MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-25 for ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY TFFB-36-95-ZT manufactured by Cook Inc.
Report Number | 1820334-2020-00684 |
MDR Report Key | 9880090 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-25 |
Date of Report | 2020-03-25 |
Date of Event | 2020-03-10 |
Date Mfgr Received | 2020-03-10 |
Device Manufacturer Date | 2019-02-18 |
Date Added to Maude | 2020-03-25 |
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 | MRS. JENNIFER CANADA |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal | 47404 |
Manufacturer Phone | 8123392235 |
Manufacturer G1 | COOK INC |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal Code | 47404 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY |
Generic Name | MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT |
Product Code | MIH |
Date Received | 2020-03-25 |
Returned To Mfg | 2020-03-20 |
Model Number | NA |
Catalog Number | TFFB-36-95-ZT |
Lot Number | 9508774XX |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK INC |
Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-25 |