Catalog Number

-

Brand Name

neocote

Version/Model Number

neocote

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KGN

Product Code Name

Dressing, Wound, Collagen

Public Device Record Key

7d5d0993-38f7-4cc0-83b7-94ffebb9fba5

Public Version Date

July 07, 2020

Public Version Number

3

DI Record Publish Date

April 21, 2017

Package DI Number

10813954022083

Quantity per Package

5

Contains DI Package

00813954022086

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box