← Back to catalogue
ORTA Ritch Trabeculoplasty Laser Lens
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
Ref 712
Identity
- Trade Name
- ORTA Ritch Trabeculoplasty Laser Lens EUDAMEDRitch Trabeculoplasty Laser Lens FDA UDI
- Generic Name
- Laser lens, ophthalmic, surgical FDA UDI
- Device Name
- Contact Ophthalmic EUDAMED
- Model / Reference
- 712 EUDAMEDORTA FDA UDI
Identifiers
- Catalog Number
- 712 FDA UDI
- Primary DI / UDI-DI
- 00630238007122 EUDAMEDFDA UDI
- Basic UDI-DI
- 06302381262637 EUDAMED
- Direct Marketing DI
- 00630238021333 EUDAMED
- 510(k) Number
- K862512 FDA UDI
- FDA Product Code
- HKS FDA UDI
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
- GMDN Term
- Laser lens, ophthalmic, surgical FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.1660 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
High-level Disinfectant FDA UDI
ORTA Ritch Trabeculoplasty Laser Lens by Ocular Instruments, Inc. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K862512 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 06302381262637 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ocular Instruments Inc.
- EUDAMED SRN
- US-MF-000007216
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED 32ad88ea-d05d-42be-97d0-c541b93721a6 61 fields · synced Jun 19, 2026
- FDA UDI c34bda3f-bd2d-4385-bb47-ea4cd3142f46 34 fields · synced May 30, 2026
- FDA 510(k) K862512 1 fields · synced May 18, 2026