Catalog Number

H100-HD

Brand Name

Venti.Plus

Version/Model Number

5407

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

K092687,K092687

Product Code

NHK

Product Code Name

Resuscitator,Manual,Non Self-Inflating

Public Device Record Key

1116e5d5-adac-4b76-9dc3-1321e0504917

Public Version Date

October 24, 2022

Public Version Number

5

DI Record Publish Date

September 19, 2015

Package DI Number

44710810100282

Quantity per Package

20

Contains DI Package

04710810100284

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton