Catalog Number

-

Brand Name

Inspire

Version/Model Number

IHC605

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

-

Product Code

CAT

Product Code Name

CANNULA, NASAL, OXYGEN

Public Device Record Key

09bf3591-5e43-4e43-965b-452dd9e821a5

Public Version Date

March 22, 2022

Public Version Number

3

DI Record Publish Date

November 04, 2016

Package DI Number

05060206920095

Quantity per Package

10

Contains DI Package

05060206920088

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box