MAUDE MDR 9392001
- MDR report key
- 9392001
- Report number
- 2210968-2019-90191
- Event key
- 0
- Event type
- 3
- Date received
- 2019-11-29
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 0
- Health professional
- 3
- Initial report to FDA
- 3
- Event location
- 3
Devices#
Seq, Brand, Generic table| Seq | Brand | Generic | Manufacturer | Product code | Model | Catalog | Lot | PMA | 510(k) | Implant | Evaluated | Availability |
|---|
| 1 | GYNECARE TVT OBTURATOR | MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC | ETHICON INC. | OTN | | 810081 | 3003256 | | | | *
| N |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2019-11-29 | 0 | 1. R
|
Event Narratives#
No narrative records found.