Catalog Number

-

Brand Name

DMEM/F-12, no glutamine

Version/Model Number

21331020

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KIT

Product Code Name

MEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE

Public Device Record Key

e2e6b5c1-00bf-4d2f-8ef5-f022e4c9ea38

Public Version Date

August 02, 2018

Public Version Number

3

DI Record Publish Date

August 01, 2016

Package DI Number

30190302003456

Quantity per Package

10

Contains DI Package

10190302003452

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case