Catalog Number

SMK 200

Brand Name

Via‐Guard®

Version/Model Number

SMK 200

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

JOL

Product Code Name

Catheter And Tip, Suction

Public Device Record Key

10259c46-0377-42bf-94cd-ebb915b04cf2

Public Version Date

April 20, 2020

Public Version Number

3

DI Record Publish Date

March 01, 2018

Package DI Number

10862630000310

Quantity per Package

10

Contains DI Package

00862630000313

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack