Identity
- Trade Name
- Well at Walgreens FDA UDI
- Generic Name
- Contact lens case FDA UDI
- Device Name
- Contact Lens Case intended for storage of soft (hydrophilic) rigid gas permeable (RPG) or hard contact lenses during chemical disinfection. FDA UDI
- Model / Reference
- 68013WG2 FDA UDI
- Description
- Contact Lens Case intended for storage of soft (hydrophilic) rigid gas permeable (RPG) or hard contact lenses during chemical disinfection. FDA UDI
Identifiers
- Catalog Number
- 156705 FDA UDI
- Primary DI / UDI-DI
- 00311917143873 FDA UDI
- FDA Product Code
- LRX FDA UDI
- GMDN Term
- Contact lens case FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Contact lens case
Well at Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Walgreen Co.
Sources (1)
- FDA UDI a6ab9f3c-5275-4f87-b596-7601055bfec2 35 fields · synced Jun 6, 2026