Catalog Number

-

Brand Name

Blood Collection Tube Holders

Version/Model Number

6933

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"

Yes

For Single-Use

Yes

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

KST

Product Code Name

System, Blood Collection, Vacuum-Assisted, Manual

Public Device Record Key

8f745658-225b-4e9e-a218-cfe75f10b97a

Public Version Date

May 31, 2021

Public Version Number

1

DI Record Publish Date

May 21, 2021

Package DI Number

00616784693330

Quantity per Package

4

Contains DI Package

00616784693316

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case