Catalog Number

-

Brand Name

Maveric Medical

Version/Model Number

M6018

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 30, 2099

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KST

Product Code Name

System, Blood Collection, Vacuum-Assisted, Manual

Public Device Record Key

7ecb0cfd-c778-4ed6-8bd2-23c37e710e70

Public Version Date

April 29, 2022

Public Version Number

2

DI Record Publish Date

July 30, 2020

Package DI Number

10860002576609

Quantity per Package

200

Contains DI Package

00860002576602

Package Discontinue Date

July 30, 2099

Package Status

In Commercial Distribution

Package Type

Box