Catalog Number

-

Brand Name

Aaris Acrylic Intraocular lens(IOL)

Version/Model Number

EC-3 PAL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HQL

Product Code Name

Intraocular Lens

Public Device Record Key

ecc57412-d3ad-4ef3-bc7f-4b6bd8cf23aa

Public Version Date

July 08, 2021

Public Version Number

3

DI Record Publish Date

September 23, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-