Catalog Number

-

Brand Name

Stradis Medical, LLC

Version/Model Number

HCT1CCSF-ST

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

0f0da57e-0873-4d8a-9ad7-33a0f80eaa39

Public Version Date

September 06, 2019

Public Version Number

3

DI Record Publish Date

August 13, 2019

Package DI Number

M752HCT1CCSFST5

Quantity per Package

5

Contains DI Package

M752HCT1CCSFST1

Package Discontinue Date

September 02, 2019

Package Status

Not in Commercial Distribution

Package Type

outer box