Identity
- Trade Name
- ILLUMINIX FDA UDI
- Generic Name
- Phoropter, electric FDA UDI
- Device Name
- Refractor instrument for trial lenses for subjective eye refraction examiation FDA UDI
- Model / Reference
- ESSENCE FDA UDI
- Description
- Refractor instrument for trial lenses for subjective eye refraction examiation FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860010833278 FDA UDI
- FDA Product Code
- HKN FDA UDI
- GMDN Term
- Phoropter, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1770 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Phoropter, electric
Illuminix by Illuminix Industries LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Illuminix Industries LLC
Sources (1)
- FDA UDI 2e6d44b9-e948-46b7-b85e-b88f656e5c5f 34 fields · synced Jun 1, 2026