The POCT Getein 1180 (model YJ-GP1180, brand FOREMED) is a portable immunofluorescence-based clinical analytical instrument for rapid blood testing. It is designed for point-of-care settings such as hospitals, clinics, laboratories, emergency care and field testing.
The analyzer uses immunofluorescence immunoassay methodology to detect target analytes in blood samples.
It has 7 regular test channels plus 1 emergency test channel. The emergency channel allows a priority or urgent test to be run without waiting for other queued tests to finish.
The device is designed for blood testing. Specific assays may require whole blood, serum, or plasma—refer to the instructions for each test kit to confirm the required sample type.
Turnaround time is assay-dependent. The analyzer is optimized for rapid point-of-care testing; many immunofluorescence assays return results in minutes (commonly in the 10–20 minute range). Check the specific test kit datasheet for exact times.
The Getein 1180 features a 10.1-inch LCD touchscreen with an easy-to-use interface for test selection, result review and basic device configuration.
Yes — it is designed to be portable. Single package size is 50 x 40 x 40 cm and gross weight is approximately 12.0 kg, making it suitable for transport between clinical locations. Power and battery details should be confirmed in the device specification or with the vendor.
The analyzer requires manufacturer-specified immunofluorescence test cartridges/reagents and control materials. Consumables are typically single-use per assay. Use only compatible kits validated for the YJ-GP1180 model.
Connectivity options (USB, LAN, Wi‑Fi, printer support, LIS/HIS integration) depend on the specific configuration and firmware. Confirm available interfaces and integration options with the supplier or in the technical specification sheet.
Routine cleaning, periodic quality control using manufacturer-supplied controls and regular calibration (as specified in the user manual) are recommended. The vendor provides online technical support for maintenance procedures and troubleshooting.
Operating and storage temperature/humidity ranges are provided in the device manual and may vary by reagent. Consult the product technical specifications or user manual for the exact environmental limits.
The analyzer is intended for use by trained healthcare professionals or laboratory personnel. Basic training on device operation, sample handling and interpretation of results is recommended; training and online support are available from the vendor.
It is suitable for rapid diagnostic testing in hospitals, clinics, laboratories, emergency departments and field settings. Specific assays determine the clinical applications (e.g., infectious markers, cardiac markers, hormone assays)—check available test menus.
Regulatory approvals and certifications vary by market and configuration. The product listing does not specify approvals; contact the manufacturer or supplier for current certification, registration and compliance documentation required in your region.
Online technical support is available as noted. Warranty terms, duration and on-site service options depend on the supplier or purchase agreement. Contact the vendor or authorized distributor for detailed warranty and support packages.
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