Catalog Number

61453

Brand Name

Stat Profile

Version/Model Number

Prime ES Plus

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"

-

For Single-Use

-

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

CHL

Product Code Name

Electrode measurement, blood-gases (pco2, po2) and blood ph

Public Device Record Key

4f146be3-fa42-41f9-90fb-9aa755826c03

Public Version Date

February 11, 2020

Public Version Number

1

DI Record Publish Date

February 03, 2020

Package DI Number

10385480614532

Quantity per Package

1

Contains DI Package

00385480614535

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton