MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1996-10-09 for 2360-71-000 manufactured by .
| Report Number | 1818910-1996-00033 |
| MDR Report Key | 44414 |
| Report Source | 05 |
| Date Received | 1996-10-09 |
| Date of Event | 1996-07-29 |
| Date Mfgr Received | 1996-09-13 |
| Device Manufacturer Date | 1993-01-01 |
| Date Added to Maude | 1996-10-28 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Product Code | HXO |
| Date Received | 1996-10-09 |
| Model Number | NA |
| Catalog Number | 2360-71-000 |
| Lot Number | NI |
| ID Number | NA |
| Device Availability | * |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 45337 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1996-10-09 |