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Member's Mark

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Member's Mark FDA UDI
Generic Name
Contact lens care kit FDA UDI
Device Name
Soft Contact Lens Disinfecting Solution, three 16 FL OZ Bottles, 1 Lens Case FDA UDI
Model / Reference
630396 FDA UDI
Description
Soft Contact Lens Disinfecting Solution, three 16 FL OZ Bottles, 1 Lens Case FDA UDI

Identifiers

Catalog Number
FCP-4278 FDA UDI
Primary DI / UDI-DI
00310119041222 FDA UDI
FDA Product Code
LYL FDA UDI
GMDN Term
Contact lens care kit 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

Yes

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: Contact lens care kit

Member's Mark by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contact lens care kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 20c2ec03-4306-4fc8-813b-f965a9dd8404 35 fields · synced May 31, 2026