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Zhengzhou Autobio Biotechnology Co., Ltd.

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BrandAutobio
ModelAutof ms2000
OriginHenan, China
Laser SourceSolid-state, ≥10⁹ shots lifetime, 1–1000 Hz tunable frequency
Ion Source Vacuum≤10⁻⁷ mbar
Ion Source MaintenanceAuto-cleaning cycle ≤10 min
Mass AnalyzerTitanium alloy flight tube with high thermal stability
Vacuum SystemHigh-throughput turbomolecular pump
Signal AcquisitionHigh-precision FPGA-controlled real-time digitizer
Software PlatformAI-accelerated microbial identification engine (96 samples in <5 min)
Database Coverage>1,000 genera, >5,000 species, >16,000 strains
Regulatory StatusCE-IVD compliant
Data SecurityOn-premise and cloud-deployable database options
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BrandAutobio
ModelAutof MS
OriginHenan, China
Laser Lifetime>100 million shots
Mass AnalyzerTitanium Alloy Linear TOF (1.05 m)
Vacuum SystemHigh-Throughput Turbo-Molecular Pump
Identification Speed≤0.1 s per sample (database search)
Microbial Database5,000+ species across 1,000+ genera, including filamentous fungi, anaerobic gut bacteria, and marine isolates
Nucleic Acid Detection CapacityUp to 40-plex per well
Regulatory CertificationNMPA-approved calibration and control materials
Software ComplianceAudit trail, user access control, and electronic signature support per FDA 21 CFR Part 11 requirements
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BrandAutobio
OriginHenan, China
Manufacturer TypeAuthorized Distributor
Country of ManufactureChina
ModelAutostreak S1800
Price RangeUSD 140,000 – 210,000 (FOB)
Instrument TypeFully Automated
Sample TypeLiquid (including sputum, broth cultures, urine supernatants)
Throughput180 Petri Dishes per Hour
Liquefaction Time≤5 min (sputum)
Streaking Time≤60 sec per 3 plates
Biosafety LevelIntegrated Class II Biological Safety Cabinet Architecture
FiltrationHEPA H14 (99.995% @ 0.3 µm)
DecontaminationAutomated UV-C (254 nm) cycle with timer-based scheduling
ConsumablesDisposable sterile tips and single-use inoculation brushes
LIS IntegrationASTM E1384 / HL7 v2.x compliant interface
Software ComplianceAudit trail, user access control, electronic signature support per FDA 21 CFR Part 11 requirements
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