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 2019-07-26 for EXPRESS SD RENAL/BILIARY 20188 manufactured by Boston Scientific Corporation.
Report Number | 2134265-2019-08799 |
MDR Report Key | 8831506 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-07-26 |
Date of Report | 2019-07-26 |
Date of Event | 2019-07-02 |
Date Mfgr Received | 2019-07-10 |
Device Manufacturer Date | 2019-03-08 |
Date Added to Maude | 2019-07-26 |
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 SCIMED, INC |
Manufacturer Street | TWO SCIMED PLACE |
Manufacturer City | MAPLE GROVE MN 55311 |
Manufacturer Country | US |
Manufacturer Postal Code | 55311 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EXPRESS SD RENAL/BILIARY |
Generic Name | CATHETER, BILIARY, DIAGNOSTIC |
Product Code | NIN |
Date Received | 2019-07-26 |
Model Number | 20188 |
Catalog Number | 20188 |
Lot Number | 0023456885 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
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 | 2019-07-26 |