MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 1997-03-25 for ARGON PATIENT MONITORING KIT * 041574504A manufactured by Argon Medical.
| Report Number | 1625425-1997-90002 |
| MDR Report Key | 82284 |
| Report Source | 07 |
| Date Received | 1997-03-25 |
| Date Mfgr Received | 1997-02-27 |
| Date Added to Maude | 1997-04-10 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| 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 | ARGON PATIENT MONITORING KIT |
| Generic Name | PATIENT MONITORING KIT |
| Product Code | FLN |
| Date Received | 1997-03-25 |
| Model Number | * |
| Catalog Number | 041574504A |
| Lot Number | UNK |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 81679 |
| Manufacturer | ARGON MEDICAL |
| Manufacturer Address | 1445 FLAT CREEK RD ATHENS TX 75751 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-03-25 |