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Meijer Coverlets Contact Lens Case
FDA UDIClass II (US FDA UDI)
by Meijer, Inc.
Identity
- Trade Name
- Meijer Coverlets Contact Lens Case FDA UDI
- Generic Name
- Contact lens case FDA UDI
- Device Name
- Contact Lens Case is intended for storage of soft (hydrophilic), rigid gas permeable (RGP), or hard contact lenses during chemical disinfection. FDA UDI
- Model / Reference
- 68737MJ FDA UDI
- Description
- Contact Lens Case is intended for storage of soft (hydrophilic), rigid gas permeable (RGP), or hard contact lenses during chemical disinfection. FDA UDI
Identifiers
- Catalog Number
- 3343420 FDA UDI
- Primary DI / UDI-DI
- 00708820128699 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
Meijer Coverlets Contact Lens Case by Meijer, Inc. — 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
- Meijer, Inc.
Sources (1)
- FDA UDI dc09ab1d-1230-490b-8954-48a96c3bd84a 34 fields · synced May 30, 2026