Catalog Number

I67980

Brand Name

Centurion

Version/Model Number

I67980

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

KDC

Product Code Name

INSTRUMENT, SURGICAL, DISPOSABLE

Public Device Record Key

22f2f5e8-17af-4679-a9da-9c71f9083b48

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

January 01, 2022

Package DI Number

10653160224815

Quantity per Package

20

Contains DI Package

00653160224818

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE