Catalog Number

0110U

Brand Name

KWIK-STIK™

Version/Model Number

0110U

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JTR

Product Code Name

KIT, QUALITY CONTROL FOR CULTURE MEDIA

Public Device Record Key

f231ea34-a16c-4152-b148-22fc0e6046c9

Public Version Date

May 08, 2020

Public Version Number

1

DI Record Publish Date

April 30, 2020

Package DI Number

20845357000235

Quantity per Package

2

Contains DI Package

10845357000238

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

2 Pack