Identity
- Trade Name
- Equate FDA UDI
- Generic Name
- Prescription spectacles FDA UDI
- Model / Reference
- JP8191EQCLR325 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00681131104388 FDA UDI
- FDA Product Code
- HOI FDA UDI
- GMDN Term
- Prescription spectacles FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5840 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: Prescription spectacles
Equate by Walmart Stores — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Prescription spectacles.
- BETSEY JOHNSON — FGX INTERNATIONAL INC. · Class I
- CORINNE MCCORMACK INC. — FGX INTERNATIONAL INC. · Class I
- Lilly Pulitzer — Kenmark Optical Co., Inc. · Class I
- Original Penguin — Kenmark Optical Co., Inc. · Class I
- DESIGN OPTICS — FGX INTERNATIONAL INC. · Class I
- Comfort Flex — Kenmark Optical Co., Inc. · Class I
- REEBOK — FGX INTERNATIONAL INC. · Class I
- I IMAGE — FGX INTERNATIONAL INC. · Class I
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
- Walmart Stores
Sources (1)
- FDA UDI d198d61c-e011-42bb-bb0a-3e8e9051a1bb 32 fields · synced May 31, 2026