Catalog Number

-

Brand Name

Lumipulse G Specimen Diluent 2

Version/Model Number

230985

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

-

Product Code

GIF

Product Code Name

Diluent, Blood Cell

Public Device Record Key

7202d61d-4082-420f-b44b-0f4f3f90d9de

Public Version Date

July 22, 2020

Public Version Number

3

DI Record Publish Date

July 14, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-