Catalog Number

DXTP118MT

Brand Name

DUO-FLOW®

Version/Model Number

DXTP118MT

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"

Yes

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

KNZ

Product Code Name

Accessories, a-v shunt

Public Device Record Key

8a658630-35de-413f-9468-9a10b3f7d12f

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

June 25, 2019

Package DI Number

50884908143091

Quantity per Package

5

Contains DI Package

00884908143096

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box