Catalog Number

-

Brand Name

Codan

Version/Model Number

LS 710

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)

-

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

5497b848-b6b2-4977-af5e-53f18fd65af2

Public Version Date

January 30, 2020

Public Version Number

3

DI Record Publish Date

September 28, 2016

Package DI Number

813153020449

Quantity per Package

1

Contains DI Package

10813153020446

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-