Catalog Number

32758

Brand Name

Suprasorb A+Ag

Version/Model Number

10cm x 20cm

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

Yes

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

-

FDA Premarket Submission

-

Product Code

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

9dd98cc7-b538-4a2f-a495-ecbb5174d63e

Public Version Date

October 21, 2022

Public Version Number

2

DI Record Publish Date

September 17, 2021

Package DI Number

20744084000672

Quantity per Package

6

Contains DI Package

10744084000675

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case