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 2019-07-03 for FILTERWIRE EZ 44150 manufactured by Boston Scientific Corporation.
Report Number | 2134265-2019-07747 |
MDR Report Key | 8757974 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-07-03 |
Date of Report | 2019-11-20 |
Date of Event | 2019-06-04 |
Date Mfgr Received | 2019-11-02 |
Device Manufacturer Date | 2018-07-19 |
Date Added to Maude | 2019-07-03 |
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 | JAY JOHNSON |
Manufacturer Street | TWO SCIMED PLACE |
Manufacturer City | MAPLE GROVE MN 55311 |
Manufacturer Country | US |
Manufacturer Postal | 55311 |
Manufacturer Phone | 7634942574 |
Manufacturer G1 | BOSTON SCIENTIFIC DE COSTA RICA S.R.L. |
Manufacturer Street | 2546 CALLE PRIMERA PROPARK, COYOL |
Manufacturer City | ALAJUELA |
Manufacturer Country | CS |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FILTERWIRE EZ |
Generic Name | TEMPORARY CORONARY SAPHENOUS VEIN BYPASS GRAFT FOR EMBOLIC PROTECTION |
Product Code | NFA |
Date Received | 2019-07-03 |
Returned To Mfg | 2019-09-18 |
Model Number | 44150 |
Catalog Number | 44150 |
Lot Number | 0022398856 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Address | TWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Other | 2019-07-03 |