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Bausch + Lomb

FDA UDI

Class II (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Bausch + Lomb FDA UDI
Generic Name
Contact lens wetting solution FDA UDI
Device Name
Soft Contact Lens Lubricanting and Rewetting Drops, 0.27 FL OZ FDA UDI
Model / Reference
625220 FDA UDI
Description
Soft Contact Lens Lubricanting and Rewetting Drops, 0.27 FL OZ FDA UDI

Identifiers

Catalog Number
FPC-4141 FDA UDI
Primary DI / UDI-DI
00310119052204 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

Yes

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: Contact lens wetting solution

Bausch + Lomb by Bausch & Lomb Incorporated — 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

Sources (1)

  • FDA UDI 50ef56c0-5ca4-42f9-8981-032698757ac8 34 fields · synced Jun 8, 2026