Catalog Number

039830000A

Brand Name

Vented IV Set

Version/Model Number

039830000A

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)

Yes

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

2c5845db-4261-41d7-a8d0-bb92a8e7a9e8

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 12, 2016

Package DI Number

20886333200775

Quantity per Package

10

Contains DI Package

00886333200771

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box