Catalog Number

-

Brand Name

IV Extension Set

Version/Model Number

7062

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)

Yes

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

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

db940074-219e-474a-bc2d-5c5d6deb788e

Public Version Date

January 20, 2022

Public Version Number

5

DI Record Publish Date

September 24, 2016

Package DI Number

00616784706238

Quantity per Package

4

Contains DI Package

00616784706221

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-