Catalog Number

STRK612538VTK

Brand Name

Performa®

Version/Model Number

00884450464670

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

DQO

Product Code Name

CATHETER, INTRAVASCULAR, DIAGNOSTIC

Public Device Record Key

0fbf54f9-4c2d-40df-983a-6fd754684c45

Public Version Date

November 08, 2021

Public Version Number

2

DI Record Publish Date

March 13, 2020

Package DI Number

10884450464677

Quantity per Package

5

Contains DI Package

00884450464670

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-