Catalog Number

-

Brand Name

Microstream Advance

Version/Model Number

MVIIH

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

733b3f27-e9e8-40a5-90e0-15e93d6e1532

Public Version Date

August 05, 2022

Public Version Number

4

DI Record Publish Date

January 09, 2020

Package DI Number

10884521761988

Quantity per Package

25

Contains DI Package

20884521761985

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE