MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-20 for MYO2 TINA-QUANT MYOGLOBIN GEN.2 MYO G2 manufactured by Roche Diagnostics.
| Report Number | 1823260-2019-90216 |
| MDR Report Key | 8909904 |
| Date Received | 2019-08-20 |
| 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 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MICHAEL LESLIE |
| Manufacturer Street | 9115 HAGUE ROAD |
| Manufacturer City | INDIANAPOLIS IN 46250 |
| Manufacturer Country | US |
| Manufacturer Postal | 46250 |
| Manufacturer G1 | ROCHE DIAGNOSTICS GMBH |
| Manufacturer Street | SANDHOFERSTRASSE 116 |
| Manufacturer City | MANNHEIM (BADEN-WURTTEMBERG), 68305 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 68305 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | 1823260-06/28/2019-006-C |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | MYO2 TINA-QUANT MYOGLOBIN GEN.2 |
| Generic Name | MYOGLOBIN IMMUNOLOGICAL TEST SYSTEM |
| Product Code | DDR |
| Date Received | 2019-08-20 |
| Model Number | MYO G2 |
| Lot Number | 349860, ASKU |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ROCHE DIAGNOSTICS |
| Manufacturer Address | 9115 HAGUE ROAD INDIANAPOLIS IN 46250 US 46250 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-20 |