Catalog Number

-

Brand Name

POLYPRO

Version/Model Number

8842P

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GAW

Product Code Name

Suture, Nonabsorbable, Synthetic, Polypropylene

Public Device Record Key

959419d3-eb0d-4a06-a7b4-0ccf6f5f7487

Public Version Date

February 05, 2021

Public Version Number

6

DI Record Publish Date

September 24, 2015

Package DI Number

20790986003884

Quantity per Package

12

Contains DI Package

10790986003887

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-