Catalog Number

645

Brand Name

Advocate Pen Needle 33G 4MM 100 Count

Version/Model Number

645

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)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

3aae7099-98e2-47f7-b6f4-58335c92ab3e

Public Version Date

January 04, 2022

Public Version Number

6

DI Record Publish Date

December 12, 2016

Package DI Number

10852982006153

Quantity per Package

12

Contains DI Package

00852982006156

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case