Catalog Number

-

Brand Name

Centurion

Version/Model Number

DT17055

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

Yes

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

-

FDA Premarket Submission

-

Product Code

LRS

Product Code Name

I.V. start kit

Public Device Record Key

fc365c8a-bd08-4e47-baa3-742a97fb9ad2

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

August 20, 2017

Package DI Number

00653160261615

Quantity per Package

10

Contains DI Package

10653160261612

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE