Catalog Number

650

Brand Name

Advocate Pen Needle 29G 12MM 100 Count

Version/Model Number

650

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)

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

1f013d62-736e-4fe5-9f00-3bddff180bea

Public Version Date

November 01, 2022

Public Version Number

6

DI Record Publish Date

December 12, 2016

Package DI Number

10852982006337

Quantity per Package

12

Contains DI Package

00852982006330

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

650-C