Catalog Number

PSMT1020

Brand Name

Gentrix®

Version/Model Number

PSMT1020

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 05, 2020

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

FTM

Product Code Name

Mesh, surgical

Public Device Record Key

a2fb9135-0c28-48ab-8db3-757f09153aa1

Public Version Date

June 10, 2022

Public Version Number

8

DI Record Publish Date

June 30, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-