Catalog Number

-

Brand Name

Accessory Sets

Version/Model Number

15-T-FA

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

-

Product Code

KJG

Product Code Name

Tube, Tissue Culture

Public Device Record Key

4f6149e3-dc3a-4228-914a-87f89348bc7b

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

20816203023067

Quantity per Package

25

Contains DI Package

10816203023060

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case