Catalog Number

-

Brand Name

Humidifier Adaptor

Version/Model Number

0485

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

-

Product Code

KFZ

Product Code Name

Humidifier, Non-Direct Patient Interface (Home-Use)

Public Device Record Key

8e8a1bc6-0da9-42ce-9142-9f566a594176

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

May 26, 2017

Package DI Number

10709078003865

Quantity per Package

50

Contains DI Package

00709078003868

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-