Catalog Number

PAKM5NPD4/A

Brand Name

Merit PAK™

Version/Model Number

00884450275665

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

b4aaaa1c-5c62-4299-bc0f-ec557f84f36a

Public Version Date

October 11, 2021

Public Version Number

2

DI Record Publish Date

April 09, 2020

Package DI Number

10884450275662

Quantity per Package

5

Contains DI Package

00884450275665

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-