Catalog Number

STRK512538SIM2

Brand Name

Performa®

Version/Model Number

00884450408575

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

a6be668c-ab48-4471-bd4e-2082cedfc961

Public Version Date

November 08, 2021

Public Version Number

2

DI Record Publish Date

March 22, 2019

Package DI Number

10884450408572

Quantity per Package

5

Contains DI Package

00884450408575

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-