MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-11-12 for PREMIERPRO? PRESSURE INFUSION BAGS 8810/500ML manufactured by Svs Llc.
Report Number | 9309304 |
MDR Report Key | 9309304 |
Date Received | 2019-11-12 |
Date of Report | 2019-11-06 |
Date of Event | 2019-10-25 |
Report Date | 2019-11-06 |
Date Reported to FDA | 2019-11-06 |
Date Reported to Mfgr | 2019-11-12 |
Date Added to Maude | 2019-11-12 |
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 | 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 | PREMIERPRO? PRESSURE INFUSION BAGS |
Generic Name | INFUSOR, PRESSURE, FOR I.V. BAGS |
Product Code | KZD |
Date Received | 2019-11-12 |
Catalog Number | 8810/500ML |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SVS LLC |
Manufacturer Address | 14120 BALLANTYNE CORPORATE PL STE 425 CHARLOTTE NC 28277 US 28277 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-12 |