Catalog Number

00710801

Brand Name

NA

Version/Model Number

00710801

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 22, 2019

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

-

Product Code

KNT

Product Code Name

TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Public Device Record Key

a0c50187-8ec7-4535-9ff4-ba5c3364012d

Public Version Date

March 25, 2019

Public Version Number

3

DI Record Publish Date

September 17, 2016

Package DI Number

10816765010751

Quantity per Package

2

Contains DI Package

00816765010754

Package Discontinue Date

March 22, 2019

Package Status

Not in Commercial Distribution

Package Type

Box