Catalog Number

MAK401NBT/C

Brand Name

Merit MAK™

Version/Model Number

00884450144404

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"

-

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

DRE

Product Code Name

DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

Public Device Record Key

2552979c-6fb8-4212-9e34-a33097505628

Public Version Date

October 11, 2021

Public Version Number

2

DI Record Publish Date

July 17, 2019

Package DI Number

10884450144401

Quantity per Package

10

Contains DI Package

00884450144404

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-