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 2019-07-19 for SPECTRANETICS ELCA CORONARY LASER ATHERECTOMY CATHETER 110-002 manufactured by The Spectranetics Corporation.
Report Number | 1721279-2019-00126 |
MDR Report Key | 8807806 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-07-19 |
Date of Report | 2019-05-16 |
Date of Event | 2019-03-20 |
Report Date | 2005-01-01 |
Date Reported to FDA | 2005-01-01 |
Date Reported to Mfgr | 2005-01-10 |
Date Mfgr Received | 2019-06-27 |
Device Manufacturer Date | 2017-11-01 |
Date Added to Maude | 2019-07-19 |
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 | MISS CATHERINE EATON |
Manufacturer Street | 9965 FEDERAL DRIVE |
Manufacturer City | COLORADO SPRINGS CO 80921 |
Manufacturer Country | US |
Manufacturer Postal | 80921 |
Manufacturer Phone | 719447-246 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SPECTRANETICS ELCA CORONARY LASER ATHERECTOMY CATHETER |
Generic Name | ELCA |
Product Code | LPC |
Date Received | 2019-07-19 |
Returned To Mfg | 2019-06-24 |
Model Number | 110-002 |
Catalog Number | 110-002 |
Lot Number | FBM17L01A |
Device Expiration Date | 2019-11-07 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | THE SPECTRANETICS CORPORATION |
Manufacturer Address | 9965 FEDERAL DRIVE COLORADO SPRINGS CO 80921 US 80921 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 14 | 1. Other | 2019-07-19 |