Moria Ou Lc 250 Head Artificial Chamber
by Moria SA
Moria Ou Lc 250 Head Artificial Chamber (19184/250), a microkeratome (FDA Class I; FDA product code HNO, Keratome, Ac-Powered) made by Moria SA, was listed in FDA GUDID on 7 May 2024 (UDI-DI 03700483603206); the registry lists it as not in commercial distribution (GUDID) as of 23 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 | Number03700483603206 | Date7 May 2024 | StatusListed |
Official records
- AccessGUDID record 03700483603206
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Moria
- Generic name
- Microkeratome
- Model / Ref / Catalog
- OU LC 250 HEAD ARTIFICIAL CHAMBER, 19184/250
- Primary DI / UDI-DI
- 03700483603206
- FDA product code
- HNO
- GMDN term
- Microkeratome
- Device class
- Class I
- Regulation number
- 886.4370
- GUDID distribution status
- Not in Commercial Distribution
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