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Meijer

FDA UDI

Class II (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer FDA UDI
Generic Name
Multi-purpose soft contact lens solution FDA UDI
Device Name
Meijer Comfort Formula Multi-purpose Solution 12 oz FDA UDI
Model / Reference
MPSA1205ME FDA UDI
Description
Meijer Comfort Formula Multi-purpose Solution 12 oz FDA UDI

Identifiers

Catalog Number
324197 FDA UDI
Primary DI / UDI-DI
00713733806695 FDA UDI
FDA Product Code
LYL FDA UDI
GMDN Term
Multi-purpose soft contact lens 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose soft contact lens solution

Meijer by Meijer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose soft contact lens solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 54316077-e565-4a0d-b336-fefc3755d773 35 fields · synced Jun 1, 2026