MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-09 for ASPIRA DRAINAGE TRAY 4992509 manufactured by C.r. Bard, Inc..
Report Number | 8771143 |
MDR Report Key | 8771143 |
Date Received | 2019-07-09 |
Date of Report | 2019-07-08 |
Date of Event | 2019-07-05 |
Report Date | 2019-07-08 |
Date Reported to FDA | 2019-07-08 |
Date Reported to Mfgr | 2019-07-09 |
Date Added to Maude | 2019-07-09 |
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 | ASPIRA DRAINAGE TRAY |
Generic Name | APPARATUS, SUCTION, PATIENT CARE |
Product Code | DWM |
Date Received | 2019-07-09 |
Model Number | 4992509 |
Catalog Number | 4992509 |
Lot Number | RECS2716 |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | C.R. BARD, INC. |
Manufacturer Address | 8195 INDUSTRIAL BLVD. COVINGTON GA 30014 US 30014 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-09 |