The Getein 1600 is a fully-automatic bench-top immunofluorescence quantitative analyzer that uses lateral flow chromatography to provide rapid, quantitative results for a wide range of biomarkers. It is designed for hospitals, clinics and laboratories to streamline diagnostic workflows.
It uses lateral flow chromatography with immunofluorescence detection for quantitative measurement of targets on disposable assay strips.
Supported sample types include whole blood, serum, plasma, urine and fingertip blood (capillary).
The analyzer supports multiple panels including Cardiac markers (hs-cTnI, cTnI, BNP, NT-proBNP, CK-MB, Myo, H-FABP), Coagulation (D-Dimer), Inflammation (hs-CRP, PCT, SAA, IL-6), Renal (CysC, mAlb, NGAL), Diabetes (HbA1c), Thyroid (TSH, T3, T4, fT3, fT4), Tumor markers (tPSA, fPSA, AFP, CEA), Fertility/Reproduction (HCG+β, FSH, LH, AMH, Progesterone, Testosterone) and others (Ferritin, Total IgE, Anti-HCV, Anti-TP).
The system can run up to 48 samples per run and achieve up to 150 tests per hour with continuous loading. Exact turnaround per assay varies by test; consult the assay insert for per-test time.
Results are shown on a 10.4-inch LCD touch screen (1024×768) and can be printed using the internal thermal printer. Results are also stored electronically for export or network transfer.
The analyzer stores over 500,000 results. Data connectivity options include LIS/HIS integration, Wi‑Fi/4G data transmission and network printer support for electronic transfer. Check with your local distributor for specific export formats and integration services.
Yes. The system uses disposable filter tips and automated sample handling to minimize cross-contamination risk.
Reagents are barcode-recognized for reagent ID and traceability. Use validated Getein reagents and consumables; reagent lot tracking and expiry are managed via the software. Replace disposable tips and reagent cartridges per the instructions for use.
The Getein 1600 supports automatic calibration and comprehensive QC management. The software allows routine QC runs, result flagging and documented SOP workflows. Performance characteristics and recommended QC schedules are provided in the assay manuals.
Yes. The analyzer offers diversified test modes including random, batch and STAT to prioritize urgent samples while maintaining continuous loading capability.
Dimensions are 639 mm (D) × 562 mm (W) × 728 mm (H). The unit weighs approximately 45 kg. Allow additional clearance for service access and ventilation.
Specific environmental (temperature/humidity) and power requirements are provided in the installation manual and should be followed for optimal performance. Contact your supplier or consult the user manual for detailed site preparation and electrical specifications.
Getein and authorized distributors typically provide installation, user training, preventive maintenance guidance and technical support. Service contracts and on-site training options vary by region; contact your local Getein representative for details.
Regulatory approvals vary by market. Please consult Getein Biotech or your local distributor for documentation on certifications (CE, local regulatory clearances, etc.) applicable in your country and for details on clinical use compliance.
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