Biomek® i7 Hybrid (MC + Span-8) with Enclosure

Biomek® i7 Hybrid (MC + Span-8) with Enclosure

Product no. B87585

Learn more about this product on Beckman.com
Biomek® i7 Hybrid (MC + Span-8) with Enclosure
Minimum Table Support Requirements116 x 63 cm
PlatformBiomek i-Series
Pod and Tool Type1μL - 300 μL 96-Channel head, 5 μL -1200 μL 96-Channel Head, 0.5 μL - 60 μL Multichannel-384 Head, Span-8 Pod
Environmental ConditionsUp to 2000 m (6562 ft.)
Installation CategoryII
Power Requirements10 A, 100-240 VAC, 50/60 Hz
Client PC Operating SystemWindows® 10
SoftwareBiomek software, SAMI EX scheduling software, Biomek PowerPack software, Biomek Method Launcher, DART 2.0 software
Display22" controller screen
Operating Mode(s)Semi-automated, manual, controlled by operator
AutoclavableNo
Material(s)ABS Cover, Acrylic Panels, Aluminum Chassis
FinishHigh-gloss paint, Hardcoat anodized coating
Weight225 kg (496 lbs)
Width170 cm
Depth81 cm (32 in)
Height104 cm (41 in)
Package Quantity1
Humidity Restrictions20%–85% (non-condensing) at 30°C
Open Text Additional DetailsSpan-8 pod installed on the Biomek i-Series instrument (ensure the following system fluid is available: de-ionized water or distilled water). | System fluid ambient operating temperature 15°C - 30°C. Degas for 24 hours prior to system installation.
Biomek® i7 Hybrid (MC + Span-8) with Enclosure
Danaher Logo
© Beckman Coulter, Inc. All rights reserved.

Beckman Coulter, the stylized logo, and the Beckman Coulter product and service marks mentioned herein are trademarks or registered trademarks of Beckman Coulter, Inc. in the United States and other countries. All other trademarks are the property of their respective owners.

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 Reagent. Analytical and performance characteristics are not established." CE-IVD, CE: Products intended for in vitro diagnostic use and conforming to the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746. (Note: Devices may be CE marked to other directives.) 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.