Catalog Number

-

Brand Name

IV Catheter Safety Winged 24G x 3/4

Version/Model Number

035831879000

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"

Yes

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

75a5290d-07e4-4099-83bf-dbf80a8726d9

Public Version Date

July 23, 2020

Public Version Number

3

DI Record Publish Date

January 01, 2019

Package DI Number

20853620005429

Quantity per Package

4

Contains DI Package

10853620005422

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-