Catalog Number

-

Brand Name

Puragraft

Version/Model Number

PGT817B

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NBY

Product Code Name

SUTURE, SURGICAL, NONABSORBABLE, EXPANDED, POLYTETRAFLOUROETHYLENE

Public Device Record Key

aa3d7b18-7bf9-4f70-a60c-85cac0ff5351

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

February 18, 2019

Package DI Number

10848782033239

Quantity per Package

12

Contains DI Package

00848782033232

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box