MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-12 for GE VT-D H4558181J manufactured by Ge Vingmed Ultrasound As.
| Report Number | 8808969 |
| MDR Report Key | 8808969 |
| Date Received | 2019-07-12 |
| Date of Report | 2019-07-11 |
| Date of Event | 2019-06-25 |
| Date Facility Aware | 2019-06-27 |
| Report Date | 2019-07-07 |
| Date Added to Maude | 2019-07-19 |
| Event Key | 0 |
| Report Source Code | User Facility 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 | RISK MANAGER |
| 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 | GE VT-D |
| Generic Name | TEE PROBE |
| Product Code | IYN |
| Date Received | 2019-07-12 |
| Catalog Number | H4558181J |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | 15 MO |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | GE VINGMED ULTRASOUND AS |
| Manufacturer Address | HORTEN NO |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Other; 4. Required No Informationntervention; 5. Deathisabilit | 2019-07-12 |