Highlights
- Original instrumentation provided by Beckman Coulter
- 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: 24 - Basophils Count (B#), Basophils Percentage (B%)
Inquire Here for a complete list!
Specifications
| Manufacturer: | Beckman Coulter |
| Series: | LH |
| Number of Assays: | 24 |
| Sample Types: | Plasma, Whole Blood, 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 |
| Optical System: | Inquire Here |
| Optical Source: | Inquire Here |
| Histogram: | Inquire Here |
| Differential: | Inquire Here |
| Test Method: | Inquire Here |
| Reagent Type: | Inquire Here |
| Reagent System: | Inquire Here |
| Reagent Delivery: | Inquire Here |
| Configuration: | Inquire Here |
| Height: | Inquire Here |
| Width: | Inquire Here |
| Depth: | Inquire Here |
| Weight: | Inquire Here |
| Power Supply: | Inquire Here |
| Point Of Care: | Inquire Here |
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®.