Akreos AO Micro Incision Lens

Basic Information

• Brand Name: Akreos AO Micro Incision Lens
• Primary DI: 10757770502995
• Version / Model: MI60LP2650
• Catalog Number: MI60LP2650
• Company Name: Bausch & Lomb Incorporated
• Labeler DUNS: 196603781
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2015-10-27
• Public Version: 3
• Public Version Date: 2021-07-08
• Public Version Status: Update
• Public Device Record Key: faa3958b-af15-41d0-93f3-1fd5f1db33b7

Device Description

MI60LP 10.50MM +26.50

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: Yes
• Has Lot/Batch Number: No
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
HQL	Intraocular Lens	Ophthalmic	886.3600	3

GMDN Terms

Code	Name	Definition	Implantable	Status
35655	Anterior-chamber intraocular lens, pseudophakic	An optical device, generally referred to as an intraocular lens (IOL), intended to be implanted permanently in the region of the eye posterior of the cornea and anterior of the iris (anterior chamber) to replace the natural lens (crystalline lens), typically because it has been clouded by a cataract. The device is typically made of a synthetic polymer; disposable devices associated with implantation (e.g., IOL injector) may be included with the lens.	Yes	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	10757770502995	GS1