MAUDE MDR 9098088
- MDR report key
- 9098088
- Report number
- 9611594-2019-00179
- Event key
- 0
- Event type
- 3
- Date received
- 2019-09-20
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 3
- 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 | INTRODUCER KIT FOR GASTROSTOMY FEEDING TUBE, 18FR DILATOR | DH EF PERC PLACEMENT PRODUCTS | AVANOS MEDICAL INC. | KGC | 98431 | 109843103 | AA7268R04 | | | | R
| N |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2019-09-20 | 0 |
|
Event Narratives#
No narrative records found.