Catalog Number

-

Brand Name

Ventlab

Version/Model Number

PRO-6140

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

K040726,K040726

Product Code

BZD

Product Code Name

Ventilator, Non-Continuous (Respirator)

Public Device Record Key

a1234dc1-a792-49bb-9332-b9e517444f8d

Public Version Date

October 24, 2022

Public Version Number

5

DI Record Publish Date

September 27, 2016

Package DI Number

20889483110000

Quantity per Package

10

Contains DI Package

10889483110003

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box