Moptim C1
by Shenzhen CERTAINN Technology Co., Ltd.
Moptim C1 is a corneal topography system analyser (FDA Class I; FDA product code MMQ, Topographer, Corneal, Ac-Powered) made by Shenzhen CERTAINN Technology Co., Ltd., listed in FDA GUDID since 15 Aug 2025 (UDI-DI 06972039971054), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06972039971054 | Date15 Aug 2025 | StatusListed |
Official records
- AccessGUDID record 06972039971054
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Moptim
- Generic name
- Corneal topography system analyser
- Model / reference
- C1
- Primary DI / UDI-DI
- 06972039971054
- FDA product code
- MMQ
- GMDN term
- Corneal topography system analyser
- Device class
- Class I
- Regulation number
- 886.1350
- GUDID distribution status
- In Commercial Distribution
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