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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Contact lens wetting solution FDA UDI
Device Name
Soft Contact Lens Rewetting Drops, 0.5 FL OZ FDA UDI
Model / Reference
156809 FDA UDI
Description
Soft Contact Lens Rewetting Drops, 0.5 FL OZ FDA UDI

Identifiers

Primary DI / UDI-DI
00311917143514 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Contact lens wetting solution

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contact lens wetting solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 3494482f-5c3d-4a86-8228-980e838dd911 34 fields · synced May 30, 2026