Catalog Number

-

Brand Name

MIXJECT

Version/Model Number

9070120

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"

-

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

K001293,K001293,K001293

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

f2d11ed9-36f6-4eca-8041-fe8846583f92

Public Version Date

March 18, 2019

Public Version Number

5

DI Record Publish Date

May 01, 2016

Package DI Number

27290108241055

Quantity per Package

8

Contains DI Package

17290108241058

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-