Identity
- Trade Name
- EYEWEAR BY ROI SORREL BLACK FDA UDI
- Generic Name
- Spectacle frame FDA UDI
- Device Name
- 52-17-135 BLACK KAREN KANE FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 52-17-135 BLACK KAREN KANE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07484743327526 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 Sorrel Black 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 549eb0eb-34a3-4710-8d10-d37d202e180a 35 fields · synced May 30, 2026