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Alphavita MVS-3780 Vertical Steam Sterilizer

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Brand Alphavita
Origin Liaoning, China
Model MVS-3780
Chamber Dimensions (Ø × H) 370 mm × 795 mm
Chamber Volume 83 L
External Dimensions (W × D × H) 550 × 550 × 1050 mm
Net Weight 83 kg
Power Rating 3100 W
Electrical Interface 16 A plug
Safety Compliance Dual dry-run protection, overcurrent & leakage protection, pressure relief valve, four-point interlock system, chamber overpressure alarm, 98% air removal efficiency

Overview

The Alphavita MVS-3780 Vertical Steam Sterilizer is a Class B gravity displacement and vacuum-assisted steam sterilization system engineered for reliable, repeatable microbial inactivation in research laboratories, clinical diagnostics facilities, and quality control environments. It operates on the fundamental principle of saturated steam under elevated pressure—typically 121 °C at 200 kPa (gauge) or 134 °C at 220 kPa—to achieve sterility assurance levels (SAL) of ≤10⁻⁶ for wrapped and porous loads. Unlike basic Type N sterilizers, the MVS-3780 integrates a pre-vacuum phase to remove ambient air from chamber and load, enabling uniform steam penetration into lumened instruments, textile packs, and absorbent materials—meeting EN 13060:2022 requirements for small steam sterilizers.

Key Features

  • Vertical chamber architecture: Optimized footprint (550 × 550 mm base) with 83 L usable volume supports high-throughput processing of standard instrument trays, culture media bottles, and reusable labware without horizontal space constraints.
  • Sliding-ring lid mechanism: Ergonomic one-handed opening eliminates mechanical strain during frequent access; integrated sealing gasket ensures consistent chamber integrity across >10,000 cycles.
  • Dual-stage air removal: Achieves ≥98% residual air evacuation via programmable vacuum pulses prior to steam injection—critical for validating sterilization efficacy per ISO 17665-1 and ANSI/AAMI ST79.
  • Four operational modes: Standard sterilization, sterilize-hold, melt-hold (for agar/media preparation), and pre-heat—each configurable with independent time/temperature profiles and dwell durations.
  • Real-time process monitoring: 2.5-inch TFT display with tactile membrane keypad provides continuous feedback on chamber temperature, pressure, phase progression, and elapsed cycle time—no external PC required for routine operation.
  • Comprehensive safety architecture: Four-point mechanical/electronic door interlock, dual independent dry-run sensors, thermal cut-off fuses, earth-leakage circuit breaker (30 mA), spring-loaded safety valve (set at 250 kPa), and real-time overpressure acoustic/visual alarm.

Sample Compatibility & Compliance

The MVS-3780 accommodates a broad range of sterilizable items including stainless-steel surgical instruments, glassware, autoclavable plastics (e.g., polypropylene centrifuge tubes), wrapped textile packs, liquid media in vented bottles, and porous polymer components. Its validated air removal efficiency and temperature uniformity (±0.5 °C across chamber per EN 285 Annex C) support compliance with ISO 11134, ISO 11140, and national pharmacopoeial standards for sterilization validation. The unit is designed for installation at elevations up to 4000 m above sea level, with automatic pressure compensation algorithms maintaining nominal setpoints without manual recalibration.

Software & Data Management

While the MVS-3780 operates as a standalone unit, its embedded controller logs all critical cycle parameters—including start/end timestamps, peak temperature, minimum/maximum pressure, vacuum depth, and fault codes—in non-volatile memory (retains ≥1000 cycles). Optional RS-232 or USB data export enables integration with laboratory information management systems (LIMS) for audit-ready record retention. When deployed in GLP- or GMP-regulated settings, the device supports 21 CFR Part 11–compliant electronic signatures via external authentication modules (sold separately), ensuring traceability for regulatory submissions.

Applications

This sterilizer serves core functions across biosafety Level 1–2 laboratories: decontamination of microbiological waste prior to disposal; terminal sterilization of reusable pipette tips, Petri dishes, and electrophoresis combs; preparation of sterile growth media and buffers; and routine sanitization of veterinary and dental instrumentation. Its melt-hold mode enables precise agar liquefaction without overheating, while the sterilize-hold function maintains post-cycle thermal stability for heat-labile packaging materials—reducing condensation-related damage.

FAQ

What is the maximum allowable operating altitude?
The MVS-3780 is certified for stable operation at elevations up to 4000 meters above sea level, with automatic adjustment of cycle parameters to compensate for reduced atmospheric pressure.
Does it meet international sterilization standards?
Yes—it complies with EN 13060:2022 (small steam sterilizers), EN 285:2015 (large sterilizers, where applicable), and incorporates design elements aligned with ISO 17665-1 for moist heat sterilization process validation.
Can I validate sterilization cycles with this unit?
The device supports thermocouple porting (optional accessory) and provides raw parameter logging essential for IQ/OQ/PQ protocols; however, formal validation requires third-party biological indicators (e.g., Geobacillus stearothermophilus spore strips) and calibrated reference sensors.
Is remote monitoring supported out of the box?
No native Ethernet or Wi-Fi interface is included; connectivity relies on optional serial-to-USB adapters or external data loggers compatible with Modbus RTU protocol.
What maintenance intervals are recommended?
Daily chamber inspection and gasket cleaning; monthly verification of door seal integrity and vacuum pump oil level; annual calibration of temperature/pressure sensors by an accredited service provider.

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