Catalog Number

H5TF-010

Brand Name

LifeGlobal® Media

Version/Model Number

H5TF-010

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

K142991

Product Code

MQL

Product Code Name

MEDIA, REPRODUCTIVE

Public Device Record Key

db733dc8-1268-4140-86bf-e3f7af123fae

Public Version Date

March 15, 2019

Public Version Number

2

DI Record Publish Date

February 28, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-