Catalog Number

-

Brand Name

Stradis Medical, LLC.

Version/Model Number

HCT900ABP

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

PEZ

Product Code Name

Central Venous Catheter Dressing Change Kit

Public Device Record Key

6a69ae38-580f-4edc-ac17-b8709699a494

Public Version Date

October 06, 2020

Public Version Number

4

DI Record Publish Date

December 12, 2017

Package DI Number

M752HCT900ABP5

Quantity per Package

30

Contains DI Package

M752HCT900ABP0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer box