MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-11-26 for UNKNOWN manufactured by W.l. Gore & Associates.
| Report Number | 3003910212-2019-00490 |
| MDR Report Key | 9379500 |
| Date Received | 2019-11-26 |
| Date of Report | 2019-11-22 |
| Date of Event | 2012-10-05 |
| Date Added to Maude | 2019-11-26 |
| 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 | HEIDI WOMBLE |
| Manufacturer Phone | 9285263030 |
| Manufacturer G1 | MPD APC B/P |
| Manufacturer Street | P.O. BOX 1408 |
| Manufacturer City | ELKTON MD 219221408 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 219221408 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | UNKNOWN |
| Product Code | OWT |
| Date Received | 2019-11-26 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | W.L. GORE & ASSOCIATES |
| Manufacturer Address | FLAGSTAFF AZ |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-11-26 |