Moria Ou Lc 450 Head Artificial Chamber
by Moria SA
Moria Ou Lc 450 Head Artificial Chamber (19184/450) is a microkeratome (FDA Class I; FDA product code HNO, Keratome, Ac-Powered) made by Moria SA, listed in FDA GUDID since 7 May 2024 (UDI-DI 03700483603398), registry data 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 | Number03700483603398 | Date7 May 2024 | StatusListed |
Official records
- AccessGUDID record 03700483603398
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Moria
- Generic name
- Microkeratome
- Model / Ref / Catalog
- OU LC 450 HEAD ARTIFICIAL CHAMBER, 19184/450
- Primary DI / UDI-DI
- 03700483603398
- FDA product code
- HNO
- GMDN term
- Microkeratome
- Device class
- Class I
- Regulation number
- 886.4370
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HNO (Keratome, Ac-Powered).
- ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS by Lasersight Technologies, Inc.
- Treatment Pack (Size M) 1014 by Carl Zeiss Meditec AG
- MICROKERATOME, MODEL MK-2000 by Nidek, Inc.
- AUTOMATED DISPOSABLE KERATOME (ADK) by Lasersight Technologies, Inc.
- MODIFICATION TO CIBA VISION CENTURION SES SPIKERATOME by Ciba Vision Corporation
- MICROKERATOME OR THE MATE by Howard Instruments, Inc.
- Treatment Packs (Size M) 1462-333 by Carl Zeiss Meditec AG
- BLADEWORKS MICROKERATOME BLADE, MODEL 7061 by Blade Works, Inc.
- INNOVATOME MICROKERATOME by Innovative Optics, Inc.
- MODIFICATION TO VISITOME 20-10 MICROKERATOME by Biovision, Inc.