Catalog Number

-

Brand Name

Health Mart

Version/Model Number

052569134955

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NAC

Product Code Name

Dressing, Wound, Hydrophilic

Public Device Record Key

f17ccbb1-f66d-4fa0-b54b-fff2a60d6316

Public Version Date

August 24, 2021

Public Version Number

2

DI Record Publish Date

July 31, 2020

Package DI Number

20052569134959

Quantity per Package

72

Contains DI Package

00052569134955

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case