Specifications
| Minimum Table Support Requirements | #N/A / #N/A |
| Platform | Biomek 4000 |
| Environmental Conditions | Up to 2000 m |
| Installation Category | II |
| Sterile | No |
| Power Requirements | 100-240 VAC, 50/60 Hz, 10 A |
| Operating System | Windows® 7 |
| Software | Biomek software, SAMI EX scheduling software, Biomek PowerPack software, Biomek Method Launcher, DART 2.0 software |
| Display | 22" controller screen |
| Operating Mode(s) | Semi-automated, manual, controlled by operator |
| Autoclavable | No |
| Material(s) | Aluminum chassis, ABS Cover |
| Finish | Spatter-coat paint, stainless steel |
| Weight | 40.8 kg / 90 lb |
| Width | 122.5 cm / 48.2 in |
| Depth | 50.5 cm / 19.9 in |
| Height | 67.5 cm / 26.6 in |
| Package Quantity | 1 |
| Temperature Range | 5°C - 30°C |
| Humidity Restrictions | < 85% (non-condensing) at 30°C |
NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES
PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS
The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.