Alalis AS06 Touchscreen Ultrasonic Cleaner

Overview

The Alalis AS06 Touchscreen Ultrasonic Cleaner is a precision-engineered benchtop cleaning system designed for laboratories requiring consistent, non-destructive removal of particulate, organic, and oily contaminants from delicate or geometrically complex components. It operates on the principle of ultrasonic cavitation: high-frequency sound waves (40 kHz) generate microscopic vacuum bubbles in the cleaning solution, which collapse violently near solid surfaces—producing localized energy sufficient to dislodge adherent residues without mechanical abrasion or thermal stress. Engineered for reproducibility and operational stability, the AS06 delivers uniform energy distribution across its 6-liter stainless-steel tank, making it suitable for routine cleaning of glassware, surgical instruments, optical lenses, microfluidic devices, and semiconductor wafers. Its compliance with international safety and electromagnetic compatibility standards—including UL/CSA recognition and IEC 61000-6-3—ensures safe integration into regulated laboratory environments.

Key Features

• Precision capacitive touchscreen interface with intuitive icon-based navigation, enabling rapid parameter selection and real-time status feedback.
• Adjustable ultrasonic output (40–100% of nominal 150 W), allowing optimization of cleaning intensity for sensitive substrates or heavily soiled samples.
• Dedicated degassing mode to remove dissolved air from cleaning solutions prior to operation—enhancing cavitation efficiency and reducing cycle variability.
• Non-heating design ensures thermally labile samples remain within ambient temperature limits; ideal for applications where thermal degradation must be avoided.
• Robust 304 stainless-steel tank with electropolished interior surface resists corrosion from aqueous and mild solvent-based cleaning agents.
• Integrated self-diagnostic system continuously monitors transducer load, power delivery, and thermal conditions—triggering automatic shutdown upon detection of overload or abnormal temperature rise.
• Memory retention function preserves user-defined timer settings and power levels after power interruption, eliminating repeated configuration.
• Vibration-isolating rubber feet provide mechanical stability on uneven or resonant work surfaces, minimizing energy loss and acoustic feedback.

Sample Compatibility & Compliance

The AS06 accommodates a broad range of sample geometries—including hollow tubes, threaded fittings, porous ceramics, and MEMS assemblies—without requiring manual agitation or scrubbing. Its 300 × 150 × 150 mm internal tank volume supports standard laboratory glassware (e.g., volumetric flasks up to 1 L, Petri dishes, pipette tips) and small industrial components. The unit meets essential regulatory expectations for cleanroom-adjacent use: housing features corrosion-resistant powder-coated steel construction compliant with ISO 14644-1 Class 7 particulate requirements when operated under controlled ventilation. While not certified for sterile processing per ISO 13485 or FDA 21 CFR Part 820, it is routinely deployed in pre-sterilization cleaning workflows aligned with AAMI ST79 and USP guidelines. No drain valve or lid is included, reflecting its intended use in closed-loop, single-batch cleaning protocols where solution reuse or containment is not required.

Software & Data Management

The AS06 operates via embedded firmware with no external PC dependency. All operational parameters—including elapsed time, remaining time, and active power level—are displayed in real time on the high-contrast touchscreen. Although the device does not support data export, audit trail logging, or electronic signature functionality, its deterministic behavior and hardware-level parameter locking ensure procedural consistency across operators and shifts. For laboratories operating under GLP or GMP frameworks, the AS06 may be integrated into broader equipment qualification protocols (IQ/OQ/PQ) using standardized test methods such as ASTM D2603 (cavitation intensity mapping) and ISO 13074 (ultrasonic cleaner performance verification). Firmware updates are performed manually via USB port (not included), with version history traceable through the system’s diagnostic menu.

Applications

• Pre-analytical preparation of HPLC vials, GC liners, and autosampler needles in analytical chemistry labs.
• Cleaning of endoscopic accessories and reusable biopsy forceps in clinical pathology departments.
• Removal of photoresist residue and metal particulates from silicon wafers during microfabrication R&D.
• Decontamination of cell culture inserts, transwell membranes, and microtiter plates in life science research.
• Restoration of antique optical components and museum-grade instrumentation prior to metrological calibration.
• Supporting ASTM E1947 (standard practice for ultrasonic cleaning of metals) and ISO 11553-1 (safety requirements for ultrasonic equipment).

FAQ

Does the AS06 include a heating function?

No. The AS06 is a non-heating ultrasonic cleaner. Temperature control is not available, ensuring compatibility with heat-sensitive materials and volatile solvents.

Can the unit be used with flammable solvents?

Only with appropriate engineering controls (e.g., explosion-proof ventilation, intrinsically safe transducers). The AS06 is rated for aqueous and mild detergent solutions; solvent compatibility must be verified against material safety data sheets and local fire codes.

Is the touchscreen compatible with gloved operation?

Yes—the capacitive interface responds reliably to standard nitrile and latex gloves, supporting use in biosafety cabinets and cleanrooms.

What maintenance is required for long-term reliability?

Routine cleaning of the tank interior with deionized water after each use; periodic inspection of transducer mounting integrity; annual verification of ultrasonic output using calibrated hydrophone or aluminum foil test per ASTM E1000.

Does the AS06 meet FDA 21 CFR Part 11 requirements?

No. It lacks electronic recordkeeping, audit trails, or user authentication capabilities. It is intended for non-GxP-critical cleaning steps unless validated as part of a larger controlled process.