Catalog Number

99407

Brand Name

Sterrad

Version/Model Number

99407

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

-

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

LRP

Product Code Name

TRAY, SURGICAL

Public Device Record Key

9e931af0-2a51-4b55-9417-29a61b5de8c7

Public Version Date

September 16, 2022

Public Version Number

7

DI Record Publish Date

May 31, 2018

Package DI Number

20705037043177

Quantity per Package

4

Contains DI Package

10705037043170

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case