Catalog Number

9004476

Brand Name

Henry Schein

Version/Model Number

9004476

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

FMF

Product Code Name

Syringe, piston

Public Device Record Key

82941478-92bb-4dfd-b392-40853e3e0da8

Public Version Date

November 09, 2020

Public Version Number

5

DI Record Publish Date

September 24, 2016

Package DI Number

10304040002879

Quantity per Package

4

Contains DI Package

00304040002872

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box