Catalog Number

106C0

Brand Name

Kashi Scientific

Version/Model Number

2112

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

KXG

Product Code Name

Applicator, Absorbent Tipped, Sterile

Public Device Record Key

45c46a3d-f48d-4248-83af-51725988eae3

Public Version Date

July 15, 2022

Public Version Number

2

DI Record Publish Date

January 01, 2022

Package DI Number

00850039389603

Quantity per Package

100

Contains DI Package

00860008024459

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack