Catalog Number

-

Brand Name

Centurion

Version/Model Number

A1237

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

FMG

Product Code Name

Stopcock, i.V. Set

Public Device Record Key

30601076-bc84-4838-a791-380460df4579

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

October 04, 2018

Package DI Number

00653160321135

Quantity per Package

50

Contains DI Package

10653160321132

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE