Catalog Number

-

Brand Name

Parietene DS

Version/Model Number

PPDS12X3

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K163212,K163212

Product Code

FTL

Product Code Name

Mesh, surgical, polymeric

Public Device Record Key

2ab964f3-5a0e-4195-9cfd-81b8dcf8c3d3

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

January 26, 2020

Package DI Number

20884521784083

Quantity per Package

3

Contains DI Package

10884521784086

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE