Neuvar
AF-600/300 Automated Identification and Susceptibility Testing System
Neuvar

AF-600/300 Automated Identification and Susceptibility Testing System

- Automated identification and susceptibility testing system for accurate microbial analysis.
- Utilizes a smart ID encyclopedia and expert system for reliable results on common and rare strains.
- Features multi-wavelength detection and dynamic algorithms to enhance result accuracy and speed.
- Capable of testing over 200+ antimicrobials, identifying various resistance mechanisms.
- Supports high-throughput testing with simultaneous analysis of up to 64 specimens.
- Simplifies operations with automated processes and a user-friendly 3-step workflow.

SKU
3A6B6BD409E4
Brand
Neuvar
Availability
In stock
  • Warranty included
  • Worldwide shipping
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Clinical overview

Product overview

Automated identification and susceptibility testing system

AF-600/300

 
When comprehensive ID/AST panel meets accurate results and a smart workflow
Smart
 
  • • ID encyclopedia: Provides morphology and culture, pathogenicity and epidemiological information of common strains to help laboratories verify the accuracy of ID results when 2 or 3 ID results accounts;
  • • Expert system: Indicates rare antimicrobial resistance, conflict antimicrobial susceptibility results and other information (Phenotype and treatment related) based on CLSI/EUCAST/FDA rules and several clinical guidelines;
 
Accurate
 
  • • Multi-wavelength detection: A five-wavelength detection system is adopted to accurately match the characteristic wavelengths of different biochemical chromogenic reactions to obtain more specific interpretation data and improve the accuracy of results;
  • • Dynamic detection: The intelligent dynamic recognition algorithm is used to perform cyclic dynamic (20min) interpretation of the test card, which not only improves the accuracy of the results, but also improves the timeliness of the detection. The results can be produced in 4 to 5 hours at the fastest, which greatly shortens the TAT.
 
Comprehensive
 
  • • More then 200 + antimicrobials;
  • • Estimation of susceptibility based on serial double microbroth dilution of MICs in line with CLSI and EUCAST guidelines, without skipping the dilution of antibiotics;
  • • Identify various emerging resistance mechanisms that may be present in samples, including MRSA, BORSA, MRCoNS, VISA, hVISA, VRSA, VRE, HLGR, CRE, CRAB, CRPAE, MLSb, PRSP, PISP, and BLNAR.
 
High throughput and automation
High-throughput: can accommodate 32/64 specimens for simultaneous testing, and can be inspected at any time; Automation: Automatic dynamic interpretation, automatic collection, automatic self-inspection, etc. during the test card detection process, greatly optimizing the detection process.
Software management
Data reporting management: Data file formats approved by WHONET can be exported with one click, without the need for other software conversion; Data statistics management: Provides multi-dimensional statistical methods, including bacterial detection rate, antibiotic resistance rate, resistance trend, multiple drug resistance phenotypes, inspection submission rate, workload and other dimensions.
Unique incubation mode
The use of tower constant temperature circulation incubation channels allows each well on the test card to obtain a fast and stable incubation environment, greatly improving the accuracy of detection.
Unique test card structure
The frustum-shaped test hole structure design is more conducive to bacterial growth and aggregation and simplifies manual interpretation.
Simple operation in 3 steps
Type of ID/AST combined panels
* On development

Available on request

Configuration, paperwork & clinical fit

The full spec + documentation pack for this device ships ahead of purchase on request. A sales engineer responds within one business day.

Configuration sheet

Specifications, accessories & clinical fit

Sizes and dimensions, material and finish, compatible instruments and screw references, what ships in the set, lead time and warranty — all in one specification sheet, sent within one business day.

Documents & downloads

Regulatory paperwork & manuals

This device's IFU, CE Declaration of Conformity, ISO 13485 certificate and (where applicable) FDA 510(k) clearance ship with the order. Reach out below for the pack ahead of purchase.

Get in touch

Need configuration help, certificates, or volume pricing?

Our clinical sales team will scope quantities, voltage, accessories and regulatory paperwork — usually within one business day.

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