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REFRESH CONTACTS® Contact Lens Comfort Drops
FDA UDIClass II (US FDA UDI)
by Allergan
Identity
- Trade Name
- REFRESH CONTACTS® Contact Lens Comfort Drops FDA UDI
- Generic Name
- Contact lens wetting solution FDA UDI
- Device Name
- REFRESH CONTACTS® Contact Lens Comfort Drops FDA UDI
- Model / Reference
- 91822US FDA UDI
- Description
- REFRESH CONTACTS® Contact Lens Comfort Drops FDA UDI
Identifiers
- Catalog Number
- 91822US FDA UDI
- Primary DI / UDI-DI
- 00300231822120 FDA UDI
- 510(k) Number
- K992028 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Contact lens wetting solution 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
No
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Contact lens wetting solution
REFRESH CONTACTS® Contact Lens Comfort Drops by Allergan — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Contact lens wetting solution.
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- Biotrue® Hydration Boost Contact Lens Rehydrating Drops — Bausch & Lomb Incorporated · 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
- Allergan
Sources (1)
- FDA UDI d33f9108-c861-49f5-b132-d71480378921 36 fields · synced May 30, 2026