Catalog Number

600

Brand Name

Advocate Pen Needle 29G 12.7MM

Version/Model Number

600

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 20, 2020

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

bc43074a-2432-4446-8675-0ae572ef2787

Public Version Date

November 01, 2022

Public Version Number

7

DI Record Publish Date

August 20, 2016

Package DI Number

10894046001520

Quantity per Package

12

Contains DI Package

00894046001523

Package Discontinue Date

July 20, 2020

Package Status

Not in Commercial Distribution

Package Type

600-C