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BenAng BA-1S Stomacher-type Homogenizer

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Brand BenAng
Origin Shanghai, China
Manufacturer Type Authorized Distributor
Country of Origin China
Model BA-1S
Instrument Type Stomacher-type (Paddle-beat) Homogenizer
Dimensions (W×D×H) 250 × 370 × 380 mm
Sample Volume Range 3–100 mL
Homogenization Time Settings 30, 60, 180, 600 s + continuous mode (5-step programmable)
Beat Frequency 2–9 beats/sec
Power Supply 220 V / 50 Hz
Power Consumption 80 W
Net Weight 18 kg
Sterile Filter Bag Size 17 × 28 cm
Safety Features Hall-effect door interlock, leak-proof waste tray, fully opening front door, transparent viewing window

Overview

The BenAng BA-1S Stomacher-type Homogenizer is a laboratory-grade mechanical homogenization system engineered for reproducible, contamination-controlled sample preparation in microbiological and analytical workflows. Operating on the principle of controlled paddle-beat action—where a motor-driven oscillating paddle applies rhythmic compressive shear forces against a sterile filter bag containing sample and diluent—the BA-1S achieves efficient liberation of microorganisms from solid or semi-solid matrices without thermal degradation or cross-contamination. This mechanism ensures uniform dispersion while preserving microbial viability and structural integrity of analytes, making it particularly suitable for quantitative microbial enumeration (e.g., colony-forming unit counts), pathogen recovery, and pre-analytical processing prior to PCR, ELISA, or culture-based assays. Designed for compliance with standard operating procedures in regulated environments, the BA-1S supports GLP-aligned sample handling and integrates seamlessly into ISO 17025-accredited laboratories performing food safety testing, pharmaceutical environmental monitoring, clinical diagnostics, and veterinary microbiology.

Key Features

  • Programmable homogenization cycles: Five discrete time settings (30 s, 60 s, 180 s, 600 s) plus continuous mode for method flexibility and protocol standardization.
  • Adjustable beat frequency: Precise control over mechanical energy input (2–9 beats per second) enables optimization for delicate tissues, viscous suspensions, or resilient biofilms.
  • Full-access front door with transparent polycarbonate window: Facilitates real-time visual monitoring of bag integrity and homogenization progress without interrupting operation.
  • Hall-effect safety interlock: Automatically halts paddle motion upon door opening, preventing operator injury and ensuring adherence to IEC 61000-6-2 and EN 61000-6-4 electromagnetic compatibility and functional safety requirements.
  • Dedicated leak containment system: Integrated waste tray captures incidental leakage from sterile bags, minimizing surface contamination and simplifying decontamination between runs.
  • No-contact sample processing: The sample remains fully enclosed within single-use, gamma-sterilized filter bags (17 × 28 cm); no internal chamber surfaces contact the specimen, eliminating carryover risk and reducing cleaning validation burden.
  • Ergonomic design: Compact footprint (250 × 370 × 380 mm) and low acoustic emission (<65 dB(A)) support placement in biosafety cabinets or shared lab spaces without disrupting adjacent instrumentation.

Sample Compatibility & Compliance

The BA-1S accommodates a broad spectrum of sample types—including raw meat, dairy products, leafy greens, soil suspensions, fecal specimens, and pharmaceutical excipients—within the 3–100 mL volume range. Its use with certified sterile filter bags complies with ISO 6887-1:2017 (microbiology of food and animal feeding stuffs — preparation of test samples), FDA Bacteriological Analytical Manual (BAM) Chapter 3 (Microbiological Methods), and USP and . All electrical components conform to CE marking directives (2014/30/EU EMC Directive and 2014/35/EU LVD Directive). The device supports audit-ready documentation when paired with laboratory information management systems (LIMS) via manual log entry; optional external timer logging can be integrated for 21 CFR Part 11-compliant environments.

Software & Data Management

The BA-1S operates via an embedded electromechanical timer interface with tactile push-button controls and LED status indicators—intentionally omitting digital firmware to ensure long-term reliability, eliminate cybersecurity exposure, and simplify IQ/OQ/PQ validation. Time and speed parameters are manually set and recorded externally per SOP. For laboratories requiring electronic recordkeeping, integration with validated LIMS or electronic lab notebooks (ELN) is achieved through standardized operator-entered metadata (e.g., sample ID, batch number, homogenization duration, beat rate, date/time stamp). No proprietary software or cloud connectivity is included, aligning with institutional IT security policies governing standalone laboratory instruments.

Applications

  • Food safety testing: Recovery of Salmonella, Listeria monocytogenes, and E. coli O157:H7 from ground beef, poultry, produce, and ready-to-eat foods.
  • Pharmaceutical QC: Microbial load assessment of non-sterile drug products and environmental swab samples per USP .
  • Clinical microbiology: Homogenization of stool, wound swabs, and tissue biopsies prior to culture or molecular detection.
  • Environmental monitoring: Processing of water filters, air sampling cassettes, and surface wipes in cleanroom and manufacturing settings.
  • Research applications: Cell lysis for DNA/RNA extraction from plant tissues or biofilm-coated substrates where enzymatic or sonication methods may cause nucleic acid shearing.

FAQ

What sterile filter bags are compatible with the BA-1S?
The BA-1S is designed for use with standard 17 × 28 cm stomacher bags meeting ASTM D8198 specifications for tensile strength and pore retention (typically 100 µm or 40 µm mesh). BenAng-certified gamma-irradiated bags are recommended for regulatory submissions.

Can the BA-1S be used for quantitative microbial recovery studies?
Yes—when operated under validated time/frequency parameters and paired with appropriate positive/negative controls, the BA-1S demonstrates ≥95% recovery efficiency for common foodborne pathogens, as verified per ISO/IEC 17025 method validation guidelines.

Is routine calibration required?
No formal calibration is mandated; however, periodic verification of beat frequency (using a calibrated tachometer) and timer accuracy (±1 s tolerance) is advised per internal quality assurance protocols.

Does the instrument meet biosafety level (BSL) requirements?
While not classified as a BSL-specific device, its sealed-bag operation and leak containment tray make it suitable for BSL-2 work when used inside a certified Class II biosafety cabinet.

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