Catalog Number

1090

Brand Name

ChitoGauze®XR PRO 3" x 4 yds

Version/Model Number

1

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

K102546,K102546

Product Code

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

a63c6bee-83c7-4ab4-8f97-9932b5a4d9f0

Public Version Date

March 10, 2021

Public Version Number

2

DI Record Publish Date

January 27, 2021

Package DI Number

50870053000136

Quantity per Package

50

Contains DI Package

00870053000131

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case