Catalog Number

-

Brand Name

Unistik

Version/Model Number

AT 0714

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMK

Product Code Name

Lancet, Blood

Public Device Record Key

0903cb6c-1c64-422a-94ec-6e7e86ba2355

Public Version Date

June 17, 2021

Public Version Number

2

DI Record Publish Date

April 16, 2020

Package DI Number

00384700714031

Quantity per Package

20

Contains DI Package

00384700714017

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case