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RephiLe Large Genie G Series Ultra-Pure Water System

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Brand RephiLe
Origin Shanghai, China
Manufacturer Type Direct Manufacturer
Product Category Domestic (China-Made)
Model Large Genie G
Price Range USD 14,000 – 43,000 (est.)
Purified Water Grade ASTM Type I (Ultra-Pure)
Resistivity ≥18.2 MΩ·cm @ 25 °C
Heavy Metals & Soluble Silica < 0.01 ppb
Total Organic Carbon (TOC) < 2 ppb (ultra-pure mode), < 30 ppb (pure water mode)
Microbial Count < 0.001 CFU/mL
Endotoxin Level < 0.001 EU/mL
Particles (>0.2 µm) None (with 0.22 µm terminal filter)

Overview

The RephiLe Large Genie G Series Ultra-Pure Water System is an integrated, modular laboratory water purification platform engineered for precision, reliability, and space-efficient operation in demanding analytical and life science environments. Utilizing a multi-stage purification architecture—comprising pre-treatment with enhanced RephiAC activated carbon, anti-scaling agents, and 5 µm depth filtration; high-rejection reverse osmosis (RO) with compact, high-flux membranes; continuous electrodeionization (EDI); dual-wavelength ultraviolet oxidation (265 nm UVC lamp); and optional RephiBio terminal ultrafiltration—the system consistently delivers ASTM Type I ultra-pure water meeting or exceeding ISO 3696:1987, CLSI EP22-A, and USP specifications. Designed for laboratories where daily water demand exceeds 30–60 L/hr yet physical footprint remains constrained, the Genie G series achieves high throughput without compromising on regulatory compliance, data integrity, or operational transparency.

Key Features

  • Modular architecture enabling flexible configuration: main unit, storage tank, and distribution module operate as interoperable subsystems under centralized control.
  • Intelligent RFID-tagged consumables (RO membranes, purification cartridges, UV lamps, terminal filters) automatically recognized by the host controller for real-time lifecycle tracking and predictive maintenance alerts.
  • 8-inch waterproof color touchscreen HMI with multilingual UI (9 languages including English and Chinese), displaying live resistivity, TOC, temperature-compensated conductivity, pressure differentials, flow rates, and component status.
  • “1+N” intelligent dispensing: single main unit supports up to N networked smart dispensing arms with adjustable flow (0.01–2.0 L/min), programmable volume delivery, and on-screen water quality verification at point-of-use.
  • UVC 265 nm mercury-free germicidal lamp with >99.99% microbial inactivation efficiency and self-diagnostic lamp intensity monitoring.
  • EDI reject stream auto-diversion logic compliant with pharmaceutical GMP requirements per Annex 1 and FDA 21 CFR Part 211; configurable enable/disable via software interface.
  • No-tool service design with color-coded, RFID-verified, and physically keyed consumable bays to prevent misinstallation and ensure GLP/GMP traceability.

Sample Compatibility & Compliance

The Large Genie G system is validated for continuous production of ultra-pure water suitable for critical applications requiring low endotoxin, nuclease-free, and particle-free water. It meets or exceeds international standards including ISO 3696 (Grade 1), ASTM D1193 (Type I), CLSI EP22-A (for clinical laboratory water), and USP (Purified Water and Water for Injection specifications when paired with RephiBio terminal filtration). All electronic records—including two years of timestamped operational logs, alarm history, calibration events, and consumable usage—are stored locally with tamper-evident encryption and exportable via USB in PDF/CSV formats compliant with FDA 21 CFR Part 11 requirements for audit trails and electronic signatures. The system supports full GLP documentation workflows and is routinely deployed in QC labs supporting ISO/IEC 17025-accredited testing.

Software & Data Management

Embedded firmware enables comprehensive data governance: automatic logging of all sensor outputs (resistivity, TOC, UV intensity, pressure, temperature), consumable installation dates and remaining service life, user access logs, and alarm resolution timestamps. Data retention spans ≥24 months with cyclic overwrite protection. RephiLink mobile application provides remote monitoring across multiple Genie G units, push notifications for maintenance windows or parameter deviations, and synchronized firmware updates. Exported reports are digitally signed, non-editable, and include metadata required for regulatory submissions—supporting seamless integration into LIMS and ELN platforms. No cloud dependency: all data resides on-device unless explicitly exported.

Applications

This system serves as primary water source for high-sensitivity instrumentation including LC-MS, ICP-MS, GC-MS, HPLC, IC, AAS, and UV-Vis spectrophotometry. It supplies water for cell culture media preparation, molecular biology reagents (e.g., PCR master mixes, sequencing buffers), electrophoresis solutions, nanoparticle synthesis, and pharmaceutical process water (Purified Water grade per USP/EP). The RephiBio terminal filter option enables production of endotoxin- and DNase/RNase-free water essential for stem cell work, monoclonal antibody purification, and diagnostic assay development. Compatible with automated analyzers (clinical chemistry, immunoassay), sterilizers, washer-disinfectors, and environmental stress chambers requiring consistent feed water quality.

FAQ

What inlet water quality is required for optimal Genie G performance?
City-supplied tap water with TDS ≤1000 ppm, temperature between 5–35 °C, and feed pressure of 0.1–0.6 MPa (1–6 bar) is recommended. Pre-filtration may be advised for high-silt or high-chlorine municipal sources.
How does the system ensure long-term resistivity stability?
Through real-time temperature compensation algorithms, continuous EDI regeneration, and dual-stage polishing (mixed-bed ion exchange + 265 nm UVC photo-oxidation), ensuring consistent ≥18.2 MΩ·cm output independent of ambient fluctuations.
Is the system compatible with existing lab infrastructure?
Yes—modular mounting options include benchtop, wall-mount, or stacked configuration atop optional reservoir/distribution modules. Standard 1/4″ compression fittings and 230 V / 50 Hz (or 115 V / 60 Hz) power input ensure global adaptability.
Can the system be validated per GMP or ISO 17025 requirements?
Absolutely—the embedded data logger, RFID-tracked consumables, audit-ready report exports, and configurable alarm thresholds align with IQ/OQ/PQ protocols and support third-party validation documentation packages.
What maintenance intervals are recommended?
Pre-filters every 3–6 months; RO membrane every 12–24 months depending on feed water quality; EDI stack every 24–36 months; UV lamp annually; RephiBio filter every 6–12 months based on usage. All intervals are tracked automatically and displayed on the HMI.

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