Publix Sterile No Rub Multi-purpose Solution

FDA UDI

Class II (US FDA UDI)

by Publix Super Markets, Inc.

Identity

Trade Name: Publix Sterile No Rub Multi-purpose Solution FDA UDI
Generic Name: Multi-purpose soft/rigid contact lens solution FDA UDI
Device Name: Multi-purpose Solution for Contact Lenses FDA UDI
Model / Reference: Not Applicable FDA UDI
Description: Multi-purpose Solution for Contact Lenses FDA UDI

Identifiers

Catalog Number: Not Applicable FDA UDI
Primary DI / UDI-DI: 00041415015760 FDA UDI
FDA Product Code: LPN FDA UDI
GMDN Term: Multi-purpose soft/rigid 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

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 12 Fluid Ounce FDA UDI

Category: Multi-purpose soft/rigid contact lens solution

Publix Sterile No Rub Multi-purpose Solution by Publix Super Markets, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Publix Super Markets, Inc.

Sources (1)

FDA UDI 89da1be9-7934-4d42-996b-e06466444d9b 36 fields · synced May 30, 2026