MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-08-20 for GAS BLENDER SYSTEM 25-40-00 manufactured by Livanova Deutschland.
| Report Number | 9611109-2019-00639 |
| MDR Report Key | 8909789 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2019-08-20 |
| Date of Report | 2019-08-20 |
| Date of Event | 2019-07-22 |
| Date Mfgr Received | 2019-07-22 |
| Date Added to Maude | 2019-08-20 |
| 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 | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | BARBARA GALASSO |
| Manufacturer Street | 14401 W. 65TH WAY |
| Manufacturer City | ARVADA CO |
| Manufacturer Country | US |
| Manufacturer G1 | LIVANOVA DEUTSCHLAND |
| Manufacturer Street | LINDBERGHSTR. 25 |
| Manufacturer City | MUNICH 80939 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 80939 |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | GAS BLENDER SYSTEM |
| Generic Name | GAS CONTROL UNIT, CARDIOPULMONARY BYPASS |
| Product Code | DTX |
| Date Received | 2019-08-20 |
| Model Number | 25-40-00 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | LIVANOVA DEUTSCHLAND |
| Manufacturer Address | LINDBERGHSTR. 25 MUNICH 80939 GM 80939 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-20 |