← Back to catalogue

Pmma (s122uv)

FDA UDI

Class III (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
PMMA (S122UV) FDA UDI
Generic Name
Anterior-chamber intraocular lens, pseudophakic FDA UDI
Device Name
anterior chamber intraocular lens +9.5D FDA UDI
Model / Reference
S122UV FDA UDI
Description
anterior chamber intraocular lens +9.5D FDA UDI

Identifiers

Catalog Number
8T095 FDA UDI
Primary DI / UDI-DI
10757770150745 FDA UDI
FDA Product Code
HQL FDA UDI
GMDN Term
Anterior-chamber intraocular lens, pseudophakic FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.3600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anterior-chamber intraocular lens, pseudophakic

Pmma (s122uv) by Bausch & Lomb Incorporated — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anterior-chamber intraocular lens, pseudophakic.

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 7e679a0a-c87c-4339-907d-95125f0ea0d4 34 fields · synced Jun 8, 2026