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 2019-10-29 for NAVIGATOR HD M0062502230 250-223 manufactured by Boston Scientific Corporation.
Report Number | 3005099803-2019-05304 |
MDR Report Key | 9249973 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-29 |
Date of Report | 2019-10-29 |
Date of Event | 2019-10-15 |
Date Mfgr Received | 2019-10-15 |
Device Manufacturer Date | 2019-06-18 |
Date Added to Maude | 2019-10-29 |
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 | CAROLE MORLEY |
Manufacturer Street | 300 BOSTON SCIENTIFIC WAY |
Manufacturer City | MARLBOROUGH MA 01752 |
Manufacturer Country | US |
Manufacturer Postal | 01752 |
Manufacturer Phone | 5086834015 |
Manufacturer G1 | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Street | 780 BROOKSIDE DRIVE |
Manufacturer City | SPENCER IN 47460 |
Manufacturer Country | US |
Manufacturer Postal Code | 47460 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NAVIGATOR HD |
Generic Name | ENDOSCOPIC ACCESS OVERTUBE, GASTROENTEROLOGY-UROLOGY |
Product Code | FED |
Date Received | 2019-10-29 |
Model Number | M0062502230 |
Catalog Number | 250-223 |
Lot Number | 0023969832 |
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 | 300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-10-29 |