Identity
- Trade Name
- ViSAGE FDA UDI
- Generic Name
- Tinted non-prescription spectacles FDA UDI
- Device Name
- • Reduces glare and eye strain • 100% UVA-UVB Lens protection FDA UDI
- Model / Reference
- 702655 FDA UDI
- Description
- • Reduces glare and eye strain • 100% UVA-UVB Lens protection FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04099100314755 FDA UDI
- FDA Product Code
- HQY FDA UDI
- GMDN Term
- Tinted non-prescription spectacles FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5850 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
ViSAGE by Aldi, Inc. — 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
- Aldi, Inc.
Sources (1)
- FDA UDI 3e7edc8f-7bfa-4df1-b0cd-9292678cc111 34 fields · synced May 30, 2026