Catalog Number

PV230010F1

Brand Name

DynaMesh

Version/Model Number

VENTRAL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

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

e53467fe-7067-4476-8a2f-71b5f7a19c46

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

May 08, 2017

Package DI Number

04250274705637

Quantity per Package

3

Contains DI Package

04250274705620

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Cardboard box