Catalog Number

-

Brand Name

Omnistream

Version/Model Number

015552

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

CCK

Product Code Name

ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

Public Device Record Key

aea3411e-13f8-472a-8548-7e5f07f54791

Public Version Date

April 15, 2022

Public Version Number

7

DI Record Publish Date

November 09, 2017

Package DI Number

20884521554068

Quantity per Package

100

Contains DI Package

10884521554061

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE