Catalog Number

-

Brand Name

Stradis Medical, LLC.

Version/Model Number

525-038

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

OFL

Product Code Name

Percutaneous Sheath Introducer Kit

Public Device Record Key

5fd3eb8a-5122-4da2-8415-518b96924e46

Public Version Date

June 17, 2022

Public Version Number

4

DI Record Publish Date

August 24, 2018

Package DI Number

M7525250385

Quantity per Package

10

Contains DI Package

M7525250380

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer carton