MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-08-23 for VICI 26930 manufactured by Veniti, Inc..
| Report Number | 2134265-2019-10207 |
| MDR Report Key | 8925002 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2019-08-23 |
| Date of Report | 2019-09-19 |
| Date of Event | 2019-07-15 |
| Date Mfgr Received | 2019-08-29 |
| Device Manufacturer Date | 2019-03-05 |
| Date Added to Maude | 2019-08-23 |
| 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 | JAY JOHNSON |
| Manufacturer Street | TWO SCIMED PLACE |
| Manufacturer City | MAPLE GROVE MN 55311 |
| Manufacturer Country | US |
| Manufacturer Postal | 55311 |
| Manufacturer Phone | 7634942574 |
| Manufacturer G1 | VENITI, INC. |
| Manufacturer Street | 4025 CLIPPER COURT |
| Manufacturer City | FREMONT CA 94538 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 94538 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VICI |
| Product Code | QAN |
| Date Received | 2019-08-23 |
| Returned To Mfg | 2019-08-20 |
| Model Number | 26930 |
| Catalog Number | 26930 |
| Lot Number | 0019020019 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | VENITI, INC. |
| Manufacturer Address | 4025 CLIPPER COURT FREMONT CA 94538 US 94538 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-23 |