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OHBG-2 Hoskins-Barkan Goniotomy Premature Lens 9mm O.D.
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
Ref 833
Identity
- Trade Name
- OHBG-2 Hoskins-Barkan Goniotomy Premature Lens 9mm O.D. EUDAMEDHoskins-Barkan Goniotomy Premature Lens 9mm O.D. FDA UDI
- Generic Name
- Gonioscope FDA UDI
- Device Name
- Contact Ophthalmic EUDAMED
- Model / Reference
- 833 EUDAMEDOHBG-2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00630238008334 EUDAMEDFDA UDI
- Basic UDI-DI
- 06302381262637 EUDAMED
- 510(k) Number
- K875114 FDA UDI
- FDA Product Code
- HJK FDA UDI
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
- GMDN Term
- Gonioscope FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 886.1385 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
OHBG-2 Hoskins-Barkan Goniotomy Premature Lens 9mm O.D. 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 | K875114 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 06302381262637 | Class I | Active |
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Manufacturer
- Manufacturer
- Ocular Instruments Inc.
- EUDAMED SRN
- US-MF-000007216
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED b2e8550e-513c-4ce6-a1cc-73eac0449647 61 fields · synced Jun 19, 2026
- FDA UDI a166da7d-d3f0-4043-83f7-0ea04f9c3fa6 33 fields · synced May 30, 2026
- FDA 510(k) K875114 1 fields · synced May 18, 2026