Identity
- Trade Name
- Clear Eyes® FDA UDI
- Generic Name
- Eye lubricant FDA UDI
- Device Name
- Contact Lens Multi-Action Relief Lubricating Eye Drops for Contact Lens Wearers FDA UDI
- Model / Reference
- CE063404, CE063104 FDA UDI
- Description
- Contact Lens Multi-Action Relief Lubricating Eye Drops for Contact Lens Wearers FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00678112653218 FDA UDI
- PMA Number
- P880056 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Eye lubricant 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye lubricant
Clear Eyes® by Medtech Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye lubricant.
- REFRESH RELIEVA FOR CONTACTS — Allergan · Class II
- SYSTANE — Alcon Laboratories, Inc. · Class II
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
- Medtech Products, Inc.
Sources (1)
- FDA UDI 88cae9b2-40ef-4923-877a-902826d15ba3 36 fields · synced May 30, 2026