Catalog Number

-

Brand Name

Centurion

Version/Model Number

2217F1ST

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

KKX

Product Code Name

Drape, surgical

Public Device Record Key

809232f2-347b-4f84-a3d0-9a800387b062

Public Version Date

December 22, 2021

Public Version Number

5

DI Record Publish Date

August 31, 2016

Package DI Number

50653160044718

Quantity per Package

50

Contains DI Package

00653160044713

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE