MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-22 for SYSTEM 2000 AR52101-EU manufactured by Arjo Hospital Equipment Ab.
| Report Number | 1419652-2019-00184 |
| MDR Report Key | 8810868 |
| Date Received | 2019-07-22 |
| Date of Report | 2019-07-22 |
| Date of Event | 2019-06-28 |
| Date Facility Aware | 2019-07-01 |
| Report Date | 2019-07-22 |
| Date Reported to FDA | 2019-07-22 |
| Date Reported to Mfgr | 2019-07-22 |
| Date Added to Maude | 2019-07-22 |
| Event Key | 0 |
| Report Source Code | Distributor report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| 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 | SYSTEM 2000 |
| Generic Name | BATH, HYDRO-MASSAGE |
| Product Code | ILJ |
| Date Received | 2019-07-22 |
| Model Number | AR52101-EU |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ARJO HOSPITAL EQUIPMENT AB |
| Manufacturer Address | VERKSTADSVAGEN 5 ESLOV, 24121 SW 24121 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2019-07-22 |