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EXC200 Automated Desktop Chemistry Analyzer Clinical Analytical Instruments

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  • Shipping Timeframes: All orders are processed within 2-5 business days (excluding weekends and holidays). After your order has been processed, the estimated delivery time is before 04 Feb, 2026, depending on customs, Please note that due to high demand, some items may experience longer shipping times, which will be communicated at order confirmation email.
  • Order Processing Time: Please allow 2-5 business days for us to process your order before it is shipped . Orders placed after 16:00 on Fridays, or during weekends and public holidays, will begin processing on the next business day. Processing times may be extended during peak seasons or sales events.
  • Manufacturing Time: Some products needs manufacturing time, the manufacturing process will take approximately 10-30 business days depending on the product. This timeframe may vary depending on the complexity of the product and current demand. but this will be communicated with you during order confirmation.
  • Returns and Exchanges: We offer a 30-day return policy for most items. If you are not completely satisfied with your purchase, you may return it within 30 days of receipt for a refund or exchange. Items must be unused, in their original packaging, and accompanied by proof of purchase. Return shipping costs are the responsibility of the customer, unless the item was damaged or defective upon arrival.
1. What is the Zybio EXC200 Automated Desktop Chemistry Analyzer?

The Zybio EXC200 is a Class II automated desktop immunoassay system designed for clinical and research laboratories. It provides automated testing, a user-friendly interface, compact desktop placement, and online technical support to streamline immunoassay workflows.

2. What types of tests can the EXC200 perform?

The EXC200 is an immunoassay system intended for a range of immunoassay-based clinical and research tests. The exact assays available depend on the reagent kits and protocols provided by Zybio or approved third-party suppliers—check the current assay menu with your vendor.

3. Which sample types are compatible with the analyzer?

Many immunoassays run on common clinical sample types such as serum and plasma; compatibility with whole blood, urine, or other matrices depends on the specific assay. Confirm required sample types for each assay in the product documentation or with Zybio support.

4. What is the throughput or time-to-result for assays on the EXC200?

Throughput and time-to-result vary by assay type, protocol, and system configuration. The EXC200 is designed for fast automated testing, but for specific turnaround and samples-per-hour figures, consult the product specifications or contact Zybio for benchmarking data.

5. What level of accuracy and reliability can I expect?

The EXC200 is engineered for high accuracy and reliable performance when operated according to manufacturer instructions and using validated reagents and calibrators. Routine quality control and maintenance are required to maintain performance and documented accuracy.

6. What regulatory classification does the instrument have?

The Zybio EXC200 is listed as an Instrument Classification Class II. For use in your region, confirm regulatory clearance/registration (CE, FDA, local approvals) with Zybio or your authorized distributor.

7. How large is the instrument and is it suitable for a small lab bench?

The EXC200 has a compact desktop design intended for placement on laboratory benches. Exact dimensions and weight are provided in the technical datasheet—review those details to ensure it fits your available workspace.

8. What consumables and reagents does the EXC200 require?

The analyzer uses assay-specific reagent kits, calibrators, and quality control materials. Zybio supplies validated reagents for the EXC200; using approved consumables is recommended to ensure performance and maintain warranty coverage.

9. What are the routine maintenance and cleaning requirements?

Routine maintenance typically includes daily startup/shutdown checks, reagent and waste management, periodic cleaning of sample paths and exterior surfaces, and scheduled preventive maintenance. Follow the operator manual and the manufacturer's maintenance schedule for exact tasks and intervals.

10. How is calibration and quality control handled?

The EXC200 supports calibration and quality control procedures as required for immunoassay testing. Use manufacturer-recommended calibrators and QC materials, run QC at defined intervals, and follow the instrument's calibration workflows and documentation for compliance.

11. What software and connectivity options are available?

The EXC200 features a user-friendly interface for operation. It typically supports standard laboratory data management options—such as local data export, USB, and laboratory information system (LIS) connectivity—however, exact connectivity protocols and software features should be confirmed with Zybio or in the technical manual.

12. Is training available for operating the analyzer?

Yes. Zybio and authorized distributors generally provide operator training, including instrument setup, routine operation, maintenance, and QC procedures. Online technical support is also available for troubleshooting and guidance.

13. What technical support and warranty options are offered?

The product description notes online technical support availability. Warranty terms, service contracts, and onsite support options vary by region and distributor—contact Zybio or your authorized reseller for details on warranty length, coverage, and service plans.

14. Can the EXC200 be used for research, clinical diagnostics, and pharmaceutical testing?

Yes. The EXC200 is suitable for clinical laboratories, research facilities, healthcare institutions, pharmaceutical testing, and educational settings. Ensure intended use aligns with local regulatory requirements and that assays selected are validated for your specific application.

15. What safety and compliance considerations should users follow?

Users must follow standard laboratory biosafety practices, manufacturer safety instructions, and local regulations when handling patient samples and reagents. Proper training, use of personal protective equipment, correct waste disposal, and adherence to instrument maintenance and QC procedures are required for safe and compliant operation.

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