Identity
- Trade Name
- Anse de Snellen EUDAMEDMORIA FDA UDI
- Generic Name
- Lens loop, reusable FDA UDI
- Device Name
- Snellen Loop EUDAMEDIntended to remove the lens in cataract surgery FDA UDI
- Model / Reference
- 247 EUDAMEDSnellen Loop FDA UDI
- Description
- Intended to remove the lens in cataract surgery FDA UDI
Identifiers
- Catalog Number
- 247 FDA UDI
- Primary DI / UDI-DI
- 03700483604012 EUDAMEDFDA UDI
- Basic UDI-DI
- 37004836Loops2P EUDAMED
- Direct Marketing DI
- 03700483604012 EUDAMED
- FDA Product Code
- JYQ FDA UDI
- EMDN Code
- L1799 OPHTHALMOLOGY INSTRUMENTS, REUSABLE- OTHER EUDAMED
- GMDN Term
- Lens loop, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Anse de Snellen by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 37004836Loops2P | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Moria S.A.
- EUDAMED SRN
- FR-MF-000000336
Sources (2)
- EUDAMED 836dec9c-07c3-4364-8fae-ab0f5e1a992d 61 fields · synced Jul 28, 2026
- FDA UDI 44eeff32-4e96-431f-8efa-f6d656f15d96 34 fields · synced May 30, 2026