Catalog Number

MAG1-2030

Brand Name

InoMesh

Version/Model Number

MAG1-2030

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

8f20a2d2-42b6-4130-83cf-48687c77274d

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

December 28, 2015

Package DI Number

MDLXMAG120303

Quantity per Package

12

Contains DI Package

MDLXMAG120300

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-