MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-17 for ASTRAL 150 - DEU 27053 manufactured by Resmed Ltd.
| Report Number | 3007573469-2019-00288 |
| MDR Report Key | 9079930 |
| Date Received | 2019-09-17 |
| Date of Report | 2019-11-26 |
| Date Facility Aware | 2019-10-31 |
| Report Date | 2019-11-26 |
| Date Reported to FDA | 2019-11-26 |
| Date Reported to Mfgr | 2019-11-26 |
| Date Mfgr Received | 2019-10-31 |
| Date Added to Maude | 2019-09-17 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| 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 | ASTRAL 150 - DEU |
| Product Code | NOU |
| Date Received | 2019-09-17 |
| Returned To Mfg | 2019-08-22 |
| Model Number | 27053 |
| Catalog Number | 27053 |
| Operator | LAY USER/PATIENT |
| Device Availability | R |
| Device Age | 63 MO |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | RESMED LTD |
| Manufacturer Address | 1 ELIZABETH MACARTHUR DRIVE. BELLA VISTA SYDNEY, NSW 2153 AU 2153 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-09-17 |