Catalog Number

599600R501

Brand Name

SUPER TORQUE

Version/Model Number

599600R501

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

DQO

Product Code Name

CATHETER, INTRAVASCULAR, DIAGNOSTIC

Public Device Record Key

923f0cbe-daef-4909-9879-bda33421ba77

Public Version Date

September 14, 2022

Public Version Number

4

DI Record Publish Date

October 08, 2018

Package DI Number

20705032079096

Quantity per Package

5

Contains DI Package

10705032079099

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX