Catalog Number

-

Brand Name

M24 Hematocrit Centrifuge, 220v

Version/Model Number

HEC-24HF-7502

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 05, 2019

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GKG

Product Code Name

Centrifuge, Hematocrit

Public Device Record Key

0052a433-24fe-4cc4-bfff-24937bee5b72

Public Version Date

September 08, 2022

Public Version Number

4

DI Record Publish Date

August 01, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-