Identity
- Trade Name
- MORIA FDA UDI
- Generic Name
- Microkeratome FDA UDI
- Model / Reference
- OU LC 200 HEAD ARTIFICIAL CHAMBER FDA UDI
Identifiers
- Catalog Number
- 19184/200 FDA UDI
- Primary DI / UDI-DI
- 03700483603183 FDA UDI
- FDA Product Code
- HNO FDA UDI
- GMDN Term
- Microkeratome FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4370 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Microkeratome
Moria by Moria SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Microkeratome.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Moria SA
Sources (1)
- FDA UDI c8ed9543-d179-4cce-8924-7f86e93949d7 33 fields · synced May 29, 2026