Catalog Number

GL-NCF235BKFX

Brand Name

KODA

Version/Model Number

GL-NCF235BKFX

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

74aef82a-58a1-49cb-8b4b-57c4afa603ea

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

April 20, 2020

Package DI Number

10075289122481

Quantity per Package

10

Contains DI Package

00075289122484

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box