MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1997-11-19 for manufactured by .
| Report Number | 2020364-1997-00023 |
| MDR Report Key | 134197 |
| Date Received | 1997-11-19 |
| Date of Event | 1997-10-20 |
| Date Added to Maude | 1997-11-25 |
| 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 |
| Event Type | 3 |
| Type of Report | 3 |
| Product Code | BZW |
| Date Received | 1997-11-19 |
| Device Eval'ed by Mfgr | * |
| Implant Flag | N |
| Device Sequence No | 1 |
| Device Event Key | 131129 |
| Baseline Brand Name | ESOPHAGEAL STETHOSCOPE |
| Baseline Generic Name | STETHOSCOPE, ESOPHAGEAL |
| Baseline Model No | * |
| Baseline Catalog No | ES400-18 |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-11-19 |