MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-04 for THERMO SCIENTIFIC? TCAUTOMATION? TYPE 1020 952040 manufactured by Thermo Fisher Scientific Oy.
| Report Number | 9610942-2019-00004 |
| MDR Report Key | 8761877 |
| Date Received | 2019-07-04 |
| Date of Report | 2019-07-04 |
| Date of Event | 2019-06-11 |
| Date Mfgr Received | 2019-06-13 |
| Date Added to Maude | 2019-07-04 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | KATJA ERONEN |
| Manufacturer Street | RATASTIE 2 |
| Manufacturer City | VANTAA, 01620 |
| Manufacturer Country | FI |
| Manufacturer Postal | 01620 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | THERMO SCIENTIFIC? TCAUTOMATION? |
| Generic Name | LABORATORY AUTOMATION SYSTEM |
| Product Code | LXG |
| Date Received | 2019-07-04 |
| Model Number | TYPE 1020 |
| Catalog Number | 952040 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | THERMO FISHER SCIENTIFIC OY |
| Manufacturer Address | RATASTIE 2 VANTAA, 01620 FI 01620 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-07-04 |