Catalog Number

5622

Brand Name

TURNPIKE

Version/Model Number

IPN039139

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

DQY

Product Code Name

Catheter, percutaneous

Public Device Record Key

7d888b6e-761c-4c39-9b86-47588b463a91

Public Version Date

December 22, 2021

Public Version Number

3

DI Record Publish Date

January 14, 2020

Package DI Number

20841156105119

Quantity per Package

1

Contains DI Package

10841156105112

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box