Catalog Number

-

Brand Name

Multi-vent

Version/Model Number

3000/03DAUA001/0001

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K033008,K033008

Product Code

CAH

Product Code Name

Filter, Bacterial, Breathing-Circuit

Public Device Record Key

ba92cd38-0988-4a76-930a-a8a40991b0db

Public Version Date

September 22, 2020

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

25060120952473

Quantity per Package

12

Contains DI Package

15060120952476

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box