Catalog Number

-

Brand Name

Alleset

Version/Model Number

Model 25-FX001-S

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

FZZ

Product Code Name

MARKER, SKIN

Public Device Record Key

4fff6c30-2d76-4fce-875b-4f117f34f957

Public Version Date

February 12, 2021

Public Version Number

1

DI Record Publish Date

February 04, 2021

Package DI Number

26931918113781

Quantity per Package

100

Contains DI Package

16931918113784

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton