Catalog Number

SO-2010

Brand Name

n/a

Version/Model Number

SO-2010

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

-

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

baa74279-be50-4abf-8b3c-2cbdc766c9dc

Public Version Date

March 22, 2022

Public Version Number

3

DI Record Publish Date

November 30, 2016

Package DI Number

10607411919951

Quantity per Package

10

Contains DI Package

00607411919954

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-