Catalog Number

-

Brand Name

Stradis Medical, LLC

Version/Model Number

IM1219

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

MCY

Product Code Name

Wound Dressing Kit

Public Device Record Key

354f4c7e-ec7e-4576-8f73-2841544f698c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 14, 2017

Package DI Number

M752IM12195

Quantity per Package

20

Contains DI Package

M752IM12190

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer box