FDA Adverse Event
Summary report: N
ORTHOGAP
MDR report key: 20033
·
Received February 28, 1995
Report
- Report Number
- MW1005277
- Date Received
- February 28, 1995
- Manufacturer
- ORTHOGAP, INC.
- Product Code
- EMP
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
NO MSDS REPORT AVAILABLE. IS NOT USING FD & C APPROVED PIGMENTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ORTHOGAP | ORTHODONTIC MARKER | EMP | ORTHOGAP, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |