Identity
- Trade Name
- MORIA FDA UDI
- Generic Name
- Corneal resection holder, reusable FDA UDI
- Model / Reference
- Artificial chamber guide ring for ALTK FDA UDI
Identifiers
- Catalog Number
- 19164 FDA UDI
- Primary DI / UDI-DI
- 03700483608140 FDA UDI
- FDA Product Code
- HRH FDA UDI
- GMDN Term
- Corneal resection holder, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Corneal resection holder, reusable
Moria by Moria SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Corneal resection holder, reusable.
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- TAN-JOD DMEK BLOCK — Katena Products, Inc. · Class I
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 9c27b41e-55c4-412e-9064-0d80e7575b39 33 fields · synced May 30, 2026