Catalog Number

-

Brand Name

Invasive VentPack Mini

Version/Model Number

MP01671

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"

-

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

-

Product Code

CAI

Product Code Name

Circuit, Breathing (W Connector, Adaptor, Y Piece)

Public Device Record Key

1a6f4e9f-e759-45c7-8d82-5bade723b775

Public Version Date

December 22, 2021

Public Version Number

6

DI Record Publish Date

October 24, 2015

Package DI Number

04048675252474

Quantity per Package

10

Contains DI Package

04048675421054

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-