Catalog Number

FAS2072/B

Brand Name

Merit Medical®

Version/Model Number

00884450106990

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

K915678,K915678,K915678

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

b7e3ae39-52ac-4269-92f6-364a11f10e67

Public Version Date

April 07, 2021

Public Version Number

6

DI Record Publish Date

January 03, 2017

Package DI Number

10884450106997

Quantity per Package

25

Contains DI Package

00884450106990

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-