MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-27 for AVIATOR PLUS .014 6.0X40 142CM 4246040W manufactured by Cordis Corporation.
Report Number | 9616099-2020-03604 |
MDR Report Key | 9889468 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-27 |
Date of Report | 2020-03-27 |
Date of Event | 2020-02-26 |
Date Mfgr Received | 2020-02-26 |
Device Manufacturer Date | 2017-05-11 |
Date Added to Maude | 2020-03-27 |
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. KARLA CASTRO |
Manufacturer Street | 14201 NW 60TH AVE |
Manufacturer City | MIAMI LAKES FL 33014 |
Manufacturer Country | US |
Manufacturer Postal | 33014 |
Manufacturer Phone | 7863138372 |
Manufacturer G1 | CORDIS CORPORATION |
Manufacturer Street | 14201 NW 60TH AVE |
Manufacturer City | MIAMI LAKES FL 33014 |
Manufacturer Country | US |
Manufacturer Postal Code | 33014 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AVIATOR PLUS .014 6.0X40 142CM |
Generic Name | CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL |
Product Code | LIT |
Date Received | 2020-03-27 |
Returned To Mfg | 2020-03-19 |
Model Number | 4246040W |
Catalog Number | 4246040W |
Lot Number | 17672697 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CORDIS CORPORATION |
Manufacturer Address | 14201 NW 60TH AVE MIAMI LAKES FL 33014 US 33014 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2020-03-27 |