Catalog Number

GW1420040S

Brand Name

Traxcess SELECT

Version/Model Number

GW1420040S

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K153053

Product Code

DQX

Product Code Name

Wire, guide, catheter

Public Device Record Key

19af1254-8b1c-4b20-a0f4-cd09a4657758

Public Version Date

November 21, 2018

Public Version Number

2

DI Record Publish Date

August 07, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-