Identity
- Trade Name
- EYEWEAR BY ROI BEZ CRYSTAL GREY FDA UDI
- Generic Name
- Spectacle frame FDA UDI
- Device Name
- 49-21-145 CRYSTAL GREY RICHARD TAYLOR SCOTTSDALE FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 49-21-145 CRYSTAL GREY RICHARD TAYLOR SCOTTSDALE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07484745236628 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
- Not 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
Eyewear By Roi Bez Crystal Grey by Eyewear By Roi, Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Eyewear By Roi, Limited
Sources (1)
- FDA UDI 4d79fa3b-9d07-4ccd-b2f1-e9a2ebc15899 35 fields · synced May 31, 2026