Catalog Number

-

Brand Name

Centurion

Version/Model Number

CLPH2O001-5QB

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

ea2bc19c-e0a5-4398-beb1-510d4ede468c

Public Version Date

October 26, 2018

Public Version Number

3

DI Record Publish Date

March 23, 2017

Package DI Number

10653160308423

Quantity per Package

5

Contains DI Package

20653160308420

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE