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Akreos® AO IOL

FDA UDI

Class III (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Akreos® AO IOL FDA UDI
Generic Name
Anterior-chamber intraocular lens, pseudophakic FDA UDI
Device Name
Akreos AO Micro Incision Lens +12.00D FDA UDI
Model / Reference
MI60L FDA UDI
Description
Akreos AO Micro Incision Lens +12.00D FDA UDI

Identifiers

Catalog Number
MI60LP1200 FDA UDI
Primary DI / UDI-DI
10757770502704 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

Akreos® AO IOL 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

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Manufacturer

Manufacturer
Bausch & Lomb Incorporated

Sources (1)

  • FDA UDI fd92c891-b3ff-406a-a0f0-7e38edaf0bca 34 fields · synced Jun 8, 2026