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OI-222/GN MaxLight® Triple Two Panfundus Binocular Indirect Lens (Green)
EUDAMEDFDA UDIClass I (EU MDR)
Ref 9236
Identity
- Trade Name
- OI-222/GN MaxLight® Triple Two Panfundus Binocular Indirect Lens (Green) EUDAMEDMaxLight® Triple Two Panfundus Binocular Indirect Lens (Green) FDA UDI
- Generic Name
- Ophthalmic diagnostic condensing lens FDA UDI
- Device Name
- Indirect Lenses EUDAMED
- Model / Reference
- 9236 EUDAMEDOI-222/GN FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00630238092364 EUDAMEDFDA UDI
- Basic UDI-DI
- 06302381262739 EUDAMED
- Direct Marketing DI
- 00630238092463 EUDAMED
- FDA Product Code
- HJL FDA UDI
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
- GMDN Term
- Ophthalmic diagnostic condensing lens FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.1380 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
OI-222/GN MaxLight® Triple Two Panfundus Binocular Indirect Lens (Green) 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 | 06302381262739 | 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 da8c9ef7-d667-4b2d-a9cd-fd89037ea719 61 fields · synced Aug 4, 2026
- FDA UDI ddede86a-108f-4000-81b8-299e7c0ec99b 32 fields · synced May 30, 2026