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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
Multi-purpose rigid contact lens solution FDA UDI
Device Name
Rigid Gas Permeable Contact Lens Conditioning Solution 3.5 FL OZ FDA UDI
Model / Reference
625609 FDA UDI
Description
Rigid Gas Permeable Contact Lens Conditioning Solution 3.5 FL OZ FDA UDI

Identifiers

Catalog Number
FCP-4086 FDA UDI
Primary DI / UDI-DI
00310119056097 FDA UDI
FDA Product Code
MRC FDA UDI
GMDN Term
Multi-purpose rigid contact lens solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5918 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: Multi-purpose rigid contact lens solution

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Similar devices

Also classified as Multi-purpose rigid contact lens solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd099019-5ae4-443d-aa58-9248f75d9eac 34 fields · synced Jul 29, 2026