Catalog Number

-

Brand Name

Ventlab

Version/Model Number

4114F

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

K063813,K063813

Product Code

CCK

Product Code Name

Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Public Device Record Key

b52e03f9-6745-4bb5-bf36-1e3142dba8e5

Public Version Date

October 21, 2019

Public Version Number

3

DI Record Publish Date

September 27, 2016

Package DI Number

20889483067748

Quantity per Package

25

Contains DI Package

10889483067741

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box