Catalog Number

-

Brand Name

Endotracheal Tubes

Version/Model Number

4535

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)

-

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

ffa055a8-3943-4008-92dc-9afbdd4d3f65

Public Version Date

June 19, 2020

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

00616784453538

Quantity per Package

10

Contains DI Package

00616784453521

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-