The LS-1100 is a compact immunoassay system by Lansionbio that performs dry fluorescence (TRFIA) immunoassays for diagnostic testing in hospitals, clinics and laboratories.
The device uses time-resolved fluorescence immunoassay (TRFIA) in a dry fluorescence immunoassay format to generate sensitive and specific results.
The LS-1100 supports whole blood, plasma and serum samples.
It is designed for use in hospitals, clinics and diagnostic or research laboratories.
The instrument carries CE and ISO 13485 certifications and is classified as a Class II instrument. Users should verify local regulatory requirements for clinical use.
Single package dimensions are 37 x 33 x 25 cm and the single gross weight is 7.5 kg.
The LS-1100 is sold as a single item. Package contents (for example, power cord, starter consumables or documentation) may vary by supplier—confirm included accessories with your vendor.
The LS-1100 uses dry fluorescence immunoassay test kits/reagents compatible with the system. Specific assays, kit part numbers, and shelf life should be obtained from Lansionbio or your distributor.
The product listing includes 5 years of service and online technical support. Exact coverage terms, on-site service options and response times should be confirmed with the supplier or in the service contract.
Lansionbio or authorized distributors typically provide user training and documentation. Online technical support is available; contact your supplier to arrange training sessions or access manuals.
Calibration and maintenance schedules depend on the assays in use and local laboratory quality requirements. Follow the instrument user manual and your laboratory's QA procedures, and contact technical support for recommended routines.
Turnaround time and throughput vary by specific assay and workflow. For assay-specific timing and sample throughput figures, consult Lansionbio product literature or contact your distributor.
Connectivity and data export features are model- and configuration-dependent. Review the technical specification sheet or contact Lansionbio for details on interfaces (e.g., USB, LAN, LIS integration) and data formats.
The LS-1100 holds CE marking and ISO 13485 certification, supporting its use in clinical environments where CE conformity is required. Users must ensure compliance with local regulatory authorities before clinical diagnostic use.
Contact Lansionbio or an authorized distributor with the model number (LS-1100) and your location. Online technical support is available; provide instrument serial number and assay details to expedite assistance.
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