MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-04-14 for NAVARRE UNIVERSAL DRAINAGE CATHETER WITH NITINOL NNU 8LPT manufactured by C.r. Bard, Inc..
| Report Number | 3845011 |
| MDR Report Key | 3845011 |
| Date Received | 2014-04-14 |
| Date of Report | 2014-04-14 |
| Date of Event | 2014-02-26 |
| Report Date | 2014-04-14 |
| Date Reported to FDA | 2014-04-14 |
| Date Reported to Mfgr | 2014-06-03 |
| Date Added to Maude | 2014-06-03 |
| 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 | 0 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NAVARRE UNIVERSAL DRAINAGE CATHETER WITH NITINOL |
| Generic Name | CATHETER |
| Product Code | NWO |
| Date Received | 2014-04-14 |
| Model Number | NNU 8LPT |
| Catalog Number | NNU 8LPT |
| Lot Number | GFXG0751 |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | C.R. BARD, INC. |
| Manufacturer Address | 730 CENTRAL AVE. MURRAY HILL NJ 07974 US 07974 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-04-14 |