Catalog Number

739960

Brand Name

KENOREX

Version/Model Number

739960

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K042683,K042683,K042683

Product Code

BTR

Product Code Name

Tube, Tracheal (W/Wo Connector)

Public Device Record Key

509e4b52-b882-4a32-8a39-5261c53d5349

Public Version Date

June 19, 2020

Public Version Number

4

DI Record Publish Date

September 10, 2016

Package DI Number

20851785007081

Quantity per Package

10

Contains DI Package

10851785007084

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE