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 2019-10-15 for OUTBACK ELITE 120CM RE-ENTRY OTB59120A manufactured by Cordis Corporation.
Report Number | 9616099-2019-03274 |
MDR Report Key | 9191354 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-15 |
Date of Report | 2019-11-07 |
Date of Event | 2019-09-18 |
Date Mfgr Received | 2019-11-07 |
Device Manufacturer Date | 2019-02-26 |
Date Added to Maude | 2019-10-15 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
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 | OUTBACK ELITE 120CM RE-ENTRY |
Generic Name | CATHETER FOR CROSSING TOTAL OCCLUSIONS |
Product Code | PDU |
Date Received | 2019-10-15 |
Catalog Number | OTB59120A |
Lot Number | 17843476 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
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 | 2019-10-15 |