Catalog Number

403786

Brand Name

AQUACEL AG BURN

Version/Model Number

403786

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

K090254,K090254,K090254

Product Code

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

0a739b1b-f56f-4424-a769-87fd1b41b848

Public Version Date

May 23, 2022

Public Version Number

6

DI Record Publish Date

August 22, 2016

Package DI Number

00768455110513

Quantity per Package

5

Contains DI Package

00768455124121

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton