Catalog Number

3101-5-WO

Brand Name

MICROVAC®

Version/Model Number

3101-5-WO

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

6e14deb2-5358-47ea-b842-bd6ed291d6df

Public Version Date

August 21, 2019

Public Version Number

4

DI Record Publish Date

August 01, 2016

Package DI Number

00650551037965

Quantity per Package

12

Contains DI Package

00650551037958

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-