Catalog Number

-

Brand Name

Regard™

Version/Model Number

EY0792

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 30, 2020

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"

-

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

OJK

Product Code Name

Eye Tray

Public Device Record Key

09c5c866-8126-4d5a-9a1b-631363789c81

Public Version Date

July 31, 2020

Public Version Number

5

DI Record Publish Date

December 23, 2016

Package DI Number

20326053109014

Quantity per Package

6

Contains DI Package

10326053109017

Package Discontinue Date

July 30, 2020

Package Status

Not in Commercial Distribution

Package Type

-