Catalog Number

-

Brand Name

Stradis Medical, LLC.

Version/Model Number

169770

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"

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

-

Product Code Name

-

Public Device Record Key

21a37a70-b102-4ca2-bbc4-d45cbae06024

Public Version Date

October 06, 2020

Public Version Number

3

DI Record Publish Date

March 22, 2018

Package DI Number

M7521697705

Quantity per Package

30

Contains DI Package

M7521697700

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer box