← Back to catalogue

Boston Equalens II

FDA UDI

Class III (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Boston Equalens II FDA UDI
Generic Name
Rigid-gas-permeable corrective contact lens, extended-wear FDA UDI
Device Name
Rigid Gas Permeable Contact Lens FDA UDI
Model / Reference
oprifocon A FDA UDI
Description
Rigid Gas Permeable Contact Lens FDA UDI

Identifiers

Catalog Number
Boston Equalens II FDA UDI
Primary DI / UDI-DI
00785811435639 FDA UDI
FDA Product Code
MWL FDA UDI
NUU FDA UDI
GMDN Term
Rigid-gas-permeable corrective contact lens, extended-wear FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.5916 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthokeratology contact lensRigid-gas-permeable corrective contact lens, extended-wear

Boston Equalens II by Bausch & Lomb Incorporated — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid-gas-permeable corrective contact lens, extended-wear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bausch & Lomb Incorporated

Sources (1)

  • FDA UDI 2cce1fac-0744-4764-b2fa-6ed897ca80fa 34 fields · synced Jun 8, 2026