Catalog Number

-

Brand Name

GLOBAL HEALTHCARE

Version/Model Number

61-135

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

K042683,K042683,K042683

Product Code

BTR

Product Code Name

Tube, Tracheal (W/Wo Connector)

Public Device Record Key

a385bb71-4daa-45fc-abf2-774b78410933

Public Version Date

August 06, 2020

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

40872237005060

Quantity per Package

10

Contains DI Package

20872237005066

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE