Catalog Number

4402

Brand Name

PolyMem

Version/Model Number

Finger/Toe

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KMF

Product Code Name

Bandage, Liquid

Public Device Record Key

985ef079-ae4f-432b-b68e-00b8153a21b3

Public Version Date

September 08, 2020

Public Version Number

1

DI Record Publish Date

August 31, 2020

Package DI Number

20735471044027

Quantity per Package

6

Contains DI Package

10735471044020

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box