Catalog Number

Z7023

Brand Name

ICU Medical

Version/Model Number

Z7023

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

K082836,K082836

Product Code

FMF

Product Code Name

Syringe, piston

Public Device Record Key

10ec8585-3325-4ded-aede-28ab03db44f0

Public Version Date

September 01, 2021

Public Version Number

1

DI Record Publish Date

August 24, 2021

Package DI Number

10887709035338

Quantity per Package

50

Contains DI Package

00887709035331

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS