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Human HumaStar 300Chemistry System

Highlights

  • Original instrumentation provided by Human Diagnostics
  • Diamond Down-To-Frame® refurbishment provided.
  • Refurbishment includes disassembly and total restoration.
  • Process continues with assembly, repair, and diagnostics.
  • Certification concludes with calibration, QC and QA validation.
  • Contact Diamond for pricing, specifications and availability.

Assays

Total assays tested: 49 - Acid Phosphatase (ACP), Alanine Aminotransferase (ALT)

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Specifications

Manufacturer:Human Diagnostics
Series:HumaStar
Number of Assays:49
Sample Types:Plasma, Urine, Serum
Maximum Throughput:Inquire Here
Sample Cycle Time:Inquire Here
Sample Size Min:Inquire Here
Sample Size Max:Inquire Here
Direct Sample (STAT):Inquire Here
Auto Sample Handling:Inquire Here
Sample Input Type:Inquire Here
Sample Input Closed Tube:Inquire Here
Patient Sample Capacity:Inquire Here
Auto Dilution:Inquire Here
Assay Methodology:Inquire Here
Optical System:Inquire Here
Optical Source:Inquire Here
Test Method:Inquire Here
Reagent Type:Inquire Here
Reagent System:Inquire Here
Reagent Delivery:Inquire Here
Reagent Capacity:Inquire Here
On-Board Refrigeration:Inquire Here
Standby Mode:Inquire Here
Maintenance Free Electrodes:Inquire Here
Configuration:Inquire Here
Height:Inquire Here
Width:Inquire Here
Depth:Inquire Here
Weight:Inquire Here
Water Requirement:Inquire Here
Water OnBoard Supply:Inquire Here
Water Consumption:Inquire Here
Power Supply:Inquire Here
Point Of Care:Inquire Here

Panels

Cardiac, Electrolyte, Lipid, Liver, Metabolic, Renal

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Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 508.429.0450

Distribution Center (EU)
Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222

Quality

ISO 9001:2015 (US)
ISO 9001:2015 (EU)
ISO 13485:2016 (US)
ISO 13485:2016 (EU)

Diamond Diagnostics Inc. is registered with the United States Food and Drug Administration as an Initial Importer Manufacturer and Contract Manufacturer. Establishment registration and device listing can be found under ID: 3003030793.

Diamond has been registered with the Food and Drug Administration since 2001 and regulated by its cGMP system requirements.

All products manufactured by Diamond carry the necessary FDA clearance and comply to the European Union IVD Directive. Every department and function in our company is standardized, controlled and routinely audited.

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The names and logos of manufacturers, their instruments, and their products referred to herein may be protected by trademark or other law, and are used herein solely for purpose of reference. Products are available for international distribution only unless otherwise indicated. Diamond Diagnostics expressly disclaims any affiliation with products it does not manufacture, as well as sponsorship by other manufacturers. For current regulatory status on products within this website, please contact your sales representative. Prices and Information shown are for reference only and may change without notice. SmartLyte®, ProLyte®, CareLyte®, and Down-To-Frame® Refurbishing are Registered Trademarks of Diamond Diagnostics®.

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