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 2019-10-22 for SENTINEL CEREBRAL PROTECTION SYSTEM (US) CMS15-10C-US manufactured by Claret Medical, Inc..
Report Number | 2134265-2019-12161 |
MDR Report Key | 9220998 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-22 |
Date of Report | 2019-10-22 |
Date of Event | 2019-09-23 |
Date Mfgr Received | 2019-09-23 |
Device Manufacturer Date | 2019-07-24 |
Date Added to Maude | 2019-10-22 |
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 | JAY JOHNSON |
Manufacturer Street | TWO SCIMED PLACE |
Manufacturer City | MAPLE GROVE MN 55311 |
Manufacturer Country | US |
Manufacturer Postal | 55311 |
Manufacturer Phone | 7634942574 |
Manufacturer G1 | CLARET MEDICAL, INC. |
Manufacturer Street | 1745 COPPERHILL PARKWAY SUITE 1 |
Manufacturer City | SANTA ROSA CA 95403 |
Manufacturer Country | US |
Manufacturer Postal Code | 95403 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SENTINEL CEREBRAL PROTECTION SYSTEM (US) |
Generic Name | EMBOLIC PROTECTION DEVICE |
Product Code | PUM |
Date Received | 2019-10-22 |
Returned To Mfg | 2019-10-09 |
Model Number | CMS15-10C-US |
Catalog Number | CMS15-10C-US |
Lot Number | 19G31H27 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CLARET MEDICAL, INC. |
Manufacturer Address | 1745 COPPERHILL PARKWAY SANTA ROSA CA 95403 US 95403 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-22 |