Catalog Number

-

Brand Name

Centurion

Version/Model Number

CUHG1-5QB

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

DRS

Product Code Name

TRANSDUCER, BLOOD-PRESSURE, EXTRAVASCULAR

Public Device Record Key

f6ec4d4e-6092-485e-a71e-8c3ed18c3567

Public Version Date

October 31, 2018

Public Version Number

4

DI Record Publish Date

January 12, 2017

Package DI Number

10653160306979

Quantity per Package

5

Contains DI Package

20653160306976

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE