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Titan IS-14 Infrared Loop Sterilizer

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Brand Titan
Origin Shanghai, China
Manufacturer Type Direct Manufacturer
Region of Origin Domestic (China)
Model IS-14
Operating Temperature Range 400 °C / 850 °C
Temperature Control Mode Dual-Stage Fixed Setting
Temperature Uniformity ±50 °C
Heating Power 150 W
Internal Chamber Dimensions Φ14 mm × 150 mm

Overview

The Titan IS-14 Infrared Loop Sterilizer is a compact, benchtop dry-heat sterilization device engineered for rapid, flame-free decontamination of microbiological inoculation loops, needles, and other small metallic laboratory tools. Unlike traditional open-flame or hot-air oven methods, the IS-14 employs focused infrared radiation emitted from a high-emissivity ceramic heating element to achieve localized thermal sterilization within seconds. Its design follows the fundamental principle that sustained exposure to temperatures ≥160 °C for ≥2 minutes—or ≥180 °C for ≥30 seconds—achieves microbial inactivation via protein denaturation and nucleic acid degradation, per ISO 14937 and ASTM E2314 standards for dry-heat sterilization validation. The unit operates at two preset temperature levels—400 °C for routine loop sterilization and 850 °C for rapid carbon residue removal—enabling consistent sterility assurance without requiring external gas supply or ventilation hoods.

Key Features

  • Compact cylindrical chamber (Φ14 mm × 150 mm) optimized for standard inoculation loops and straight/curved needles up to 150 mm in length
  • Dual-stage fixed-temperature control system with tactile selector switch—no digital interface required, minimizing user error and maintenance complexity
  • Ceramic infrared emitter with high thermal inertia and stable radiant output, ensuring repeatable surface temperature profiles across repeated cycles
  • 150 W power consumption—engineered for energy efficiency and low thermal load in shared lab environments
  • Stainless steel housing with integrated heat-shielded base and front-facing safety guard to limit operator exposure during active use
  • No consumables, no calibration certificates required, and no regulatory documentation burden associated with pressurized steam systems

Sample Compatibility & Compliance

The IS-14 is validated for use with stainless steel, nickel-chromium alloy, and platinum–iridium inoculation instruments. It is not intended for sterilizing plastic, coated, or temperature-sensitive materials. While not classified as a medical device under FDA 21 CFR Part 820, the instrument supports Good Microbiological Practice (GMP) and GLP-compliant workflows when integrated into documented laboratory SOPs. Its operation aligns with ISO 13408-2 (sterility assurance for aseptic processing) and supports compliance with USP <1211> “Sterility Assurance” for non-steam-based terminal sterilization alternatives. No biological indicators are built-in; users must perform periodic verification using spore strips (e.g., Bacillus atrophaeus ATCC 9372) per ISO 11138-3.

Software & Data Management

The IS-14 is a standalone hardware-only device with no embedded microprocessor, firmware, or data logging capability. It does not feature USB, Bluetooth, or network connectivity. As such, it requires no software installation, cybersecurity validation, or 21 CFR Part 11 compliance documentation. This architecture eliminates firmware update dependencies and reduces failure modes associated with electronic controllers—making it suitable for regulated QC labs where simplicity, traceability, and audit readiness are prioritized over automation. Usage records may be maintained manually in lab notebooks or integrated into LIMS via external timestamped entries.

Applications

  • Routine sterilization of bacteriological loops and needles in clinical microbiology, food testing, and environmental monitoring labs
  • Pre- and post-inoculation tool decontamination in ISO 11133-compliant culture media preparation workflows
  • Supporting aseptic technique training in academic teaching laboratories where flame hazards must be minimized
  • Backup sterilization method during autoclave downtime or in field-deployable mobile labs with limited infrastructure
  • Complementary use alongside laminar flow hoods to maintain Class II biosafety containment integrity

FAQ

Does the IS-14 require calibration or annual certification?
No. As a fixed-temperature resistive heating device without feedback control, it is not subject to calibration requirements under ISO/IEC 17025. Users should verify performance annually using biological indicators.
Can the IS-14 sterilize glass Pasteur pipettes or plastic tips?
No. The chamber geometry and radiant heating profile are designed exclusively for metallic inoculation tools. Glass and polymer items risk thermal fracture or decomposition.
What safety standards does the housing meet?
The enclosure complies with IEC 61010-1:2010 for electrical safety in laboratory equipment, including protection against accessible hot surfaces (Class II insulation) and mechanical stability testing.
Is the IS-14 compatible with cleanroom environments (ISO 5 or better)?
Yes—provided the unit is placed outside the laminar flow zone and tools are inserted/removed using proper gowning and transfer protocols to avoid particle shedding.
How long does it take to reach operating temperature?
The emitter achieves thermal equilibrium within ≤90 seconds at 400 °C and ≤150 seconds at 850 °C, verified by thermocouple mapping per ASTM E220.

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