Biomek FXP Dual Arm System with Dual Multichannel Pipettors

A31845

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Biomek FXP Automated Liquid Handling Workstation
Includes the Biomek FXp upgraded with a dual arm system and dual multichannel pipettors. The Biomek FXp Incorporates a wide range of next-generation features in a condensed design. The Biomek FXp sets a high bar in performance and flexible laboratory solutions. It puts every aspect of liquid handling, including pipetting, dilution, dispensing and integration, into a single automated system as powerful as it is efficient and economical, while staying incredibly flexible for the changing needs of your lab. Includes our robust Biomek software and our ongoing applications development.

Specifications

Platform Biomek FX
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
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
Material(s) Aluminum chassis, ABS Cover
Finish Spatter-coat paint, stainless steel
Weight 161 kg / 354.9 lb
Width 175 cm / 68.9 in
Depth 86 cm / 33.9 in
Height 150 cm / 59.1 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.