Catalog Number

UPPL2

Brand Name

ULTRAPRO

Version/Model Number

UPPL2

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

-

Product Code

FTL

Product Code Name

Mesh, surgical, polymeric

Public Device Record Key

0f12eb7c-04dd-45d0-a268-bc380ce931b8

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

September 01, 2015

Package DI Number

20705031132426

Quantity per Package

2

Contains DI Package

10705031132429

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX