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Meijer

FDA UDI

Class II (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer FDA UDI
Generic Name
Contact lens case FDA UDI
Device Name
Contact Lens Case, Screw Top, 6 Pack FDA UDI
Model / Reference
CC18 FDA UDI
Description
Contact Lens Case, Screw Top, 6 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00713733914543 FDA UDI
FDA Product Code
LRX FDA UDI
GMDN Term
Contact lens case 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

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Contact lens case

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

Similar devices

Also classified as Contact lens case.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 18563d51-0755-4ed4-b56b-57daaf75766b 33 fields · synced May 30, 2026