MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-22 for CARDINAL HEALTH SMA12SEMWV manufactured by Cardinal Health 200, Llc.
Report Number | 9218297 |
MDR Report Key | 9218297 |
Date Received | 2019-10-22 |
Date of Report | 2019-10-07 |
Date of Event | 2019-09-09 |
Report Date | 2019-10-07 |
Date Reported to FDA | 2019-10-07 |
Date Reported to Mfgr | 2019-10-22 |
Date Added to Maude | 2019-10-22 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
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 | CARDINAL HEALTH |
Generic Name | CESAREAN SECTION TRAY |
Product Code | OHM |
Date Received | 2019-10-22 |
Model Number | SMA12SEMWV |
Catalog Number | SMA12SEMWV |
Lot Number | 538312 |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CARDINAL HEALTH 200, LLC |
Manufacturer Address | 785 FORT MILL HWY FORT MILL SC 29707 US 29707 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-22 |