Catalog Number

-

Brand Name

Stradis Medical, LLC

Version/Model Number

PMDC-2000C

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

MCY

Product Code Name

Wound Dressing Kit

Public Device Record Key

1d96aef8-6ef0-4ac2-860a-1ce4afc518bc

Public Version Date

August 20, 2018

Public Version Number

1

DI Record Publish Date

July 20, 2018

Package DI Number

M752PMDC2000C5

Quantity per Package

30

Contains DI Package

M752PMDC2000C0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer box