Catalog Number

-

Brand Name

23G x 3/4 Safety Blood Collection 12" Tubing

Version/Model Number

024441232687

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

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

e2a5c35d-766f-4f06-bdd3-65e4eb480e0e

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

January 01, 2019

Package DI Number

20853620005412

Quantity per Package

4

Contains DI Package

10853620005415

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-