Catalog Number

Hyperinflation System 0.5L with Mask

Brand Name

Venti.Plus

Version/Model Number

H050-M

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K092687,K092687

Product Code

NHK

Product Code Name

Resuscitator,Manual,Non Self-Inflating

Public Device Record Key

f5b4814e-0d93-4444-b06e-6be04c30f2d9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2015

Package DI Number

44710810100497

Quantity per Package

10

Contains DI Package

04710810100499

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton