Diamond Diagnostics offers a wide array of services to companies wishing to complement their existing product line with a Diamond product under their own branding. Diamond Diagnostics can assist interested companies with local product registrations, packaging design and well as technical, sales and support training on respective products. Diamond Diagnostics has been registered with FDA since 2001 and regulated by its cGMP system requirements. As a ISO 9001:2015 and ISO 13485:2016 certified company, all products manufactured by Diamond Diagnostics carry FDA clearance and comply to the European Union IVD Directive.
Being a vertically integrated manufacturer makes us uniquely qualified to offer the following key benefits:
- Customized Packaging and Full Color Labeling
- Individual or Bulk Packaging Options
- New Product Design, & Development and Manufacturing options available
- Internal Engineering Team
- Centralized Manufacturing, QC, and QA operations.
- Drop-Ship and Warehousing Options Available
- Direct Client Product Support Options Available
- Broad range of Regulatory, Quality and Manufacturing expertise
Click here to inquire about OEM Manufacturing
Unity ISE Module
The Diamond Diagnostics Unity Integrated Electrolyte System is a fast and compact ISE module measuring Na+, K+ and Cl- within Serum, Plasma and Diluted Urine utilizing Ion Selective Electrode (ISE) technology.
The Diamond Diagnostics Unity is uniquely designed with a powerful microprocessor and integrated electronics allowing for easy integration into any size Chemistry Analyzer platform.
Click here to Find out more about the Unity ISE Module
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
ISO 9001:2015 (US)
ISO 13485:2016 (US)
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.
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®.