Catalog Number

5513049

Brand Name

LEADER

Version/Model Number

5513049

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LPN

Product Code Name

Accessories, soft lens products

Public Device Record Key

19c51f67-078d-4cf6-9046-175a75d3a951

Public Version Date

July 02, 2021

Public Version Number

3

DI Record Publish Date

August 29, 2019

Package DI Number

50096295137083

Quantity per Package

24

Contains DI Package

00096295137088

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE