Catalog Number

SID23SFDUF

Brand Name

CARDINAL HEALTH

Version/Model Number

SID23SFDUF

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

924e62f1-25ee-4955-abf0-16cca96393b0

Public Version Date

June 17, 2022

Public Version Number

6

DI Record Publish Date

July 20, 2016

Package DI Number

50887488512783

Quantity per Package

10

Contains DI Package

10887488512785

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE