Diamond Unity®
Integrated Electrolyte System
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 Unity® is uniquely designed with a powerful microprocessor and integrated electronics allowing for easy integration into any size Chemistry Analyzer platform.
Featured Benefits
- Compact Size
- Flexible Reagent System
- Long Life Reference
- Accessible Service Area
- Fully Visible Pathway
- Fully Shielded Measurement Chamber
- Positive Engagement Latching System
- Horizontal Electrode Orientation
Built-In Modular Sample Cup Option • Accessible Service Area
| Sample | Number of Parameters | Communication | ||
| Serum or Diluted Urine | 3 (Simultaneously) | RS232 Communication | ||
| Data Storage | Calibration | Analysis Time | ||
| 2000 Patient Results | 2 Point every 8 hours | Serum: 30 sec (100 per hour) | ||
| 500 QC Results per level (3) | On Demand | Urine: 60 sec (50 per hour) | ||
| 100 Calibrations | 1 Point after every Measuremen | |||
| Sample Size | ||||
| 60 - 100 µl Serum | ||||
| 140 - 150 µl Urine | ||||
Simple Integration | ||||
 |  |  | ||
| Custom Parameter Options | Recirculating Reference Electrode | Rapid Integration | ||
Parameters and Specifications | ||||
| Parameters | Range | Reproductibility | Resolution | |||
|---|---|---|---|---|---|---|
| Serum Na+ | 50-200 mmol/L | CV ≤ 1% (120-160 mol/L) | 0.1 mmol/L | |||
| Serum K+ | 1.5-10.00 mmol/L | CV ≤ 2% (2.8-6 mmol/L) | 0.01 mmol/L | |||
| Serum CL- | 50-200 mmol/L | CV ≤ 2% (80-120 mmol/L) | 0.1 mmol/L | |||
| Urine Na+ | 20-500 mmol/L | CV ≤ 5% (60-280 mmol/L) | 1.0 mmol/L | |||
| Urine K+ | 5-300 mmol/L* | CV ≤ 5% (30-170 mmol/L) | 1.0 mmol/L | |||
| Urine CL- | 10-500 mmol/L | CV ≤ 5% (80-230 mmol/L) | 1.0 mmol/L | |||
| *(60-120) requires additional dilution | ||||||
| Power | Size & Weight | Ambient Conditions |
| 12VDC, 2.0A | 92 mm (H) x 134 mm (W) x 46 mm (D) | Room temperature: |
| (self adjusting) | or 335 x 315 x 295 mm | 15-32°C/60-90°F |
| 3.70” (H) x 5.27” (W) x 1.81” (D) | Humidity <85% | |
Literature
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 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.
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®.