Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

89-9800

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

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

4fda4c31-8208-4391-91ee-066bc27de083

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

January 21, 2018

Package DI Number

50749756945054

Quantity per Package

13

Contains DI Package

00749756945059

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case