Catalog Number

-

Brand Name

Centurion

Version/Model Number

A1247

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

ecff275f-e87a-4e18-9135-119d8767ec95

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

January 05, 2019

Package DI Number

00653160323672

Quantity per Package

50

Contains DI Package

10653160323679

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE