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OJKF Four Mirror Karickhoff Gonio Diagnostic Lens w/Flange 20mm O.D.
EUDAMEDFDA UDIClass I (EU MDR)
Ref 803
Identity
- Trade Name
- OJKF Four Mirror Karickhoff Gonio Diagnostic Lens w/Flange 20mm O.D. EUDAMEDFour Mirror Karickhoff Gonio Diagnostic Lens w/Flange 20mm O.D. FDA UDI
- Generic Name
- Gonioscope FDA UDI
- Device Name
- Contact Ophthalmic EUDAMED
- Model / Reference
- 803 EUDAMEDOJKF FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00630238008037 EUDAMEDFDA UDI
- Basic UDI-DI
- 06302381262637 EUDAMED
- Direct Marketing DI
- 00630238041287 EUDAMED
- 510(k) Number
- K862692 FDA UDI
- FDA Product Code
- HKS FDA UDI
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
- GMDN Term
- Gonioscope 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
OJKF Four Mirror Karickhoff Gonio Diagnostic Lens w/Flange 20mm O.D. by Ocular Instruments, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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 | 06302381262637 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Ocular Instruments Inc.
- EUDAMED SRN
- US-MF-000007216
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 776c4ac6-264a-4321-bbc7-d379aa693053 61 fields · synced Jun 19, 2026
- FDA UDI bb9a0694-3a59-478c-aa15-82fff1b7fc41 33 fields · synced May 30, 2026