Catalog Number

003500-0050-655

Brand Name

CT LUCIA

Version/Model Number

CT LUCIA 602.US/+11.5D

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

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"

-

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

P100016

Product Code

HQL

Product Code Name

Intraocular Lens

Public Device Record Key

8f2c49d2-bc5e-4559-88d3-4500c52451dd

Public Version Date

July 08, 2021

Public Version Number

4

DI Record Publish Date

October 01, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-