Catalog Number

DT21410

Brand Name

Centurion

Version/Model Number

DT21410

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

FYE

Product Code Name

DRESS, SURGICAL

Public Device Record Key

2eef770a-99b3-409c-81f7-0a3ff9e04adb

Public Version Date

January 10, 2022

Public Version Number

1

DI Record Publish Date

January 01, 2022

Package DI Number

00653160317602

Quantity per Package

10

Contains DI Package

10653160317609

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE