Identity
- Trade Name
- EYEWEAR BY ROI MORONI RUBY FDA UDI
- Generic Name
- Spectacle frame FDA UDI
- Device Name
- 55-16-140 RUBY BULOVA EYEWEAR FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 55-16-140 RUBY BULOVA EYEWEAR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00748474326164 FDA UDI
- FDA Product Code
- HQZ FDA UDI
- GMDN Term
- Spectacle frame FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5842 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Spectacle frame
A comprehensive guide to the Eyewear By Roi, Limited device, including its features, compliance, and FAQ.
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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
- Eyewear By Roi, Limited
Sources (1)
- FDA UDI f39bf284-6030-4384-a9c5-9122651b0d2e 34 fields · synced Jul 25, 2026