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Tabletop Dental Autoclaves

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Tabletop Dental Autoclaves are steam-based sterilization devices designed to deliver saturated steam under pressure for the purpose of killing microorganisms on instruments and materials. The design integrates a pressure vessel, steam generation, control system and safety devices to achieve repeatable sterilization cycles. Primary use scenarios include small clinics, dental practices, laboratories and other facilities requiring reliable sterilization of reusable instruments. Standard features frequently include cycle timers, temperature and pressure monitoring, automatic drying, and safety interlocks. Construction typically uses high-grade stainless steel chambers and corrosion-resistant components to support repeated exposure to steam and high temperatures. Models vary by chamber volume, cycle types, and certifications that indicate compliance with sterilization standards. Installation and operation follow documented procedures to ensure validated cycle performance and to minimize the risk of instrument damage. Regular maintenance, including periodic testing with chemical and biological indicators, supports traceability and consistent results. Technical specifications are selected to match the throughput and instrument types of the end user, balancing cycle time and energy consumption to meet workflow requirements.

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Specification

ProductTabletop Dental Autoclaves
Chamber Volume18 L / 22 L / 24 L options
Working Pressure0.12 - 0.22 MPa
Temperature Range105 - 134 °C
Power Supply220V/50Hz or 110V/60Hz
MaterialStainless steel chamber, ABS exterior
ControlElectronic timer and pressure controller

Application

Tabletop Dental Autoclaves are applied where sterilization of heat-stable instruments is required. Typical application areas include dental clinics for handpieces and mirrors, small outpatient clinics for surgical instruments, medical laboratories for glassware and metal tools, and veterinary clinics for reusable devices. In a dental setting, instruments are loaded into perforated trays and processed according to validated cycles to ensure instrument lumen and joint areas achieve required temperatures and steam penetration. Laboratory applications include sterilization of culture media containers, stainless steel tools and certain laboratory glass that tolerate high temperature and pressure. Portable and tabletop versions are suited for point-of-care sterilization where space is limited. Operational protocols often integrate pre-cleaning steps such as ultrasonic cleaning to remove gross debris prior to exposure, as residue can shield microorganisms from steam contact. Selection of specific cycle parameters depends on instrument material, lumen presence and packaging type. Record-keeping and indicator use support compliance with local regulations and internal quality systems.

Transaction Details

Accepted payment methods include wire transfer (T/T), Letter of Credit (L/C), and major international payment platforms where applicable. Order processing typically begins after receipt of confirmed payment or agreed-upon deposit. Shipping methods include sea freight, air freight, and international courier services depending on urgency and destination. Shipments are consolidated using protective packaging and secured in export-grade cartons with interior supports or pallets for larger units. Lead times vary by model and order quantity and are specified in the commercial offer. Customs documentation, certificates of origin and packing lists are prepared for export shipments. Freight terms (FOB, CIF, DDP) are negotiable at the quote stage and will be specified in the sales contract. Warranty and after-sales support terms are provided with the commercial proposal and include parts replacement guidance and service contact channels.

Advantage

The product design emphasizes consistent sterilization performance while maintaining a compact footprint suitable for limited spaces. Materials used in critical components are selected to resist corrosion and wear resulting from repeated sterilization cycles. Control systems provide documented cycle parameters that support routine verification and facilitate integration with existing practice workflows. Safety features are incorporated to prevent door opening during pressurized phases and to reduce operator exposure to hot steam. Models with automatic drying reduce instrument handling post-sterilization, lowering the risk of recontamination. Energy efficient heating and rapid recovery cycles improve throughput without adding complex maintenance requirements. Equipment architecture supports straightforward replacement of wear parts and access for service, promoting long-term uptime. Units are compatible with standard sterilization accessories and indicators used across clinical settings, enabling straightforward validation.

FAQ

  • Q: What validation methods are recommended for sterilization cycles?
  • A: Recommended validation includes the use of chemical indicators for each cycle and regular biological indicator testing according to local regulations. Record results in the maintenance log and retain certificates.
  • Q: How often should maintenance be performed?
  • A: Routine maintenance includes daily chamber cleaning, weekly gasket inspection and periodic functional checks. Follow the manufacturer maintenance schedule and retain service records.
  • Q: What packaging is compatible with steam sterilization?
  • A: Use compatible sterilization pouches or wraps designed for steam processes. Ensure packaging allows steam penetration and facilitates drying while maintaining sterility after the cycle.
  • Q: Are instruments with lumens suitable for tabletop autoclaves?
  • A: For instruments with lumens, select cycles validated for lumen penetration and follow manufacturer recommendations. Some lumen-containing instruments require longer exposures or specialized equipment.
  • Q: What safety features should operators check before use?
  • A: Confirm door locks, pressure relief valves and temperature/pressure indicators operate as intended. Verify that safety interlocks prevent opening when the chamber is pressurized.
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Wanrui Medical Instrument

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86-15728040705
86-18957491906

86-15728040705
86-18957491906