The Biomek i7 Automated Workstation has been designed to optimize dependability and walk-away time in mid- to high-throughput labs. The Biomek i7 Hybrid with enclosure has up to 45 deck positions and includes both Multichannel and Span-8 pipette heads in an enclosed work space.

Specifications

Pod and Tool Type 1μL - 300 μL 96-Channel head; 5 μL -1200 μL 96-Channel Head; 0.5 μL - 60 μL Multichannel-384 Head; Span-8 Pod
Environmental Conditions Up to 2000 m
Installation Category II
Power Requirements 100-240 VAC, 50/60 Hz, 10 A
Operating System Windows® 10
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
Material(s) ABS Cover, Acrylic panels, Aluminum chassis
Finish High-gloss paint, Hardcoat anodized coating
Weight 260 kg / 573.2 lb
Width 170 cm / 66.9 in
Depth 81 cm / 31.9 in
Height 112 cm / 44.1 in

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.