MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-05 for SAVI SCOUT? SSR75-01 manufactured by Cianna Medical, Inc..
Report Number | 8860183 |
MDR Report Key | 8860183 |
Date Received | 2019-08-05 |
Date of Report | 2019-07-15 |
Date of Event | 2019-06-11 |
Report Date | 2019-07-15 |
Date Reported to FDA | 2019-07-15 |
Date Reported to Mfgr | 2019-08-05 |
Date Added to Maude | 2019-08-05 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SAVI SCOUT? |
Generic Name | MARKER, RADIOGRAPHIC, IMPLANTABLE |
Product Code | NEU |
Date Received | 2019-08-05 |
Model Number | SSR75-01 |
Catalog Number | SSR75-01 |
Lot Number | ML04496 |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CIANNA MEDICAL, INC. |
Manufacturer Address | 6 JOURNEY, SUITE 125 ALISO VIEJO CA 92656 US 92656 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-08-05 |