Catalog Number

-

Brand Name

Centurion

Version/Model Number

SA3720KINL

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

OES

Product Code Name

Cardiac catheterization kit

Public Device Record Key

993d96da-7e41-4a2c-9e03-12c689a1c45f

Public Version Date

February 05, 2021

Public Version Number

5

DI Record Publish Date

September 14, 2016

Package DI Number

00653160247015

Quantity per Package

5

Contains DI Package

10653160247012

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE