Catalog Number

PRD500-380

Brand Name

KerraMax Care

Version/Model Number

8 x 12in

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)

-

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

fae0e8fc-e9ca-4fcd-8e65-8939b63086c3

Public Version Date

September 09, 2020

Public Version Number

3

DI Record Publish Date

October 01, 2019

Package DI Number

05060077234376

Quantity per Package

24

Contains DI Package

05060077234345

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper