Catalog Number

CVM3020US

Brand Name

COVAMESH

Version/Model Number

MSH 12 3020 V

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 26, 2016

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

ec9e7516-27e4-4605-94d8-d9c666eb86b2

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

February 26, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-