Catalog Number

-

Brand Name

MIXJECT

Version/Model Number

970133

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

-

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

K963583,K963583,K963583

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

663678de-e45b-48a5-abc3-8bf8bd324a15

Public Version Date

March 18, 2019

Public Version Number

5

DI Record Publish Date

May 01, 2016

Package DI Number

27290108241031

Quantity per Package

4

Contains DI Package

17290108241034

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-