Catalog Number

-

Brand Name

Tri-Flow

Version/Model Number

XTP3119MT

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

FOZ

Product Code Name

Catheter,intravascular,therapeutic,short-term less than 30 days

Public Device Record Key

1e8232f0-d020-4867-a795-19c9e7a4f56b

Public Version Date

February 05, 2021

Public Version Number

5

DI Record Publish Date

October 23, 2015

Package DI Number

50884908088095

Quantity per Package

5

Contains DI Package

00884908088090

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box