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Medical water treatment system

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Customization Available
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Manufacturer First
Product Attributes:
Type: Reverse Osmosis
Certification: ISO9001
Salt Rejection Rate: 99.0%
Application: Industry
Voltage: 380V
Disinfection Method: Chlorine Dioxide
Customized: Customized
Method: Biological Treatment
Usage: Home
Capacity: 80 Gallon
Control System: Fully Automatic
Treatment Process: Electrodeionization
Online Support,video Technical Support
Cleaning Method: Automated Cleaning
Filtration Capacity: 50 L/hr
Material: Stainless Steel
Motive Force: Electric power
Style: Vertical
Performance: Sophisticated Filters
Certification: RoHS
Certification: CE
Certification: FDA
Certification: GMP
Certification: ISO
Certification: GS
Certification: CB
Certification: LFGB
Certification: UR
Certification: EMF
Certification: EMC
Certification: SASO
Salt Rejection Rate: 98.5%
Salt Rejection Rate: 98.0%
Salt Rejection Rate: 99.5%
Application: Biotechnology Industry
Application: Chemical industry
Application: Clinical Diagnosis
Food & Beverage Factory
Application: Pharmaceutical Industry
Application: Food Safety
Application: Forensic Science
Water Treatment Industry
Usage: Agriculture
Usage: Hospital
Usage: Chemical Industry
Capacity: 100 Gallon
Treatment Process: Reverse Osmosis
Treatment Process: Filtration
Treatment Process: Ozonation
Treatment Process: Softening
Treatment Process: UV Disinfection

Sourcing guidance for Medical Water Treatment System

What are the core technical specifications to consider when selecting a medical water treatment system?

Buyers must prioritize systems utilizing Reverse Osmosis (RO) combined with Electrodeionization (EDI) to ensure high-purity water. Key specs include a conductivity level of <1.3 μs/cm (for USP/EP compliance), TOC (Total Organic Carbon) <500 ppb, and a bacterial count <10 CFU/100ml. Ensure the system features 316L Stainless Steel piping with orbital welding to prevent biofilm accumulation and corrosion.

Which international compliance standards are mandatory for medical-grade water systems?

The equipment must adhere to ISO 13485 (Medical Devices Quality Management) and CE marking for the European market. For clinical laboratory use, it should meet CLSI (Clinical and Laboratory Standards Institute) guidelines. If the water is for injection (WFI), the system must comply with USP <1231> or European Pharmacopoeia (Ph. Eur.) standards to ensure pyrogen-free output.

How do usage scenarios dictate the system's design and capacity?

The design varies significantly based on the application: Hemodialysis units require high-volume, continuous flow with stringent endotoxin filters; Central Sterile Supply Departments (CSSD) need high-temperature resistant components for washer-disinfectors; and Laboratory Analyzers require Type I ultra-pure water. Always calculate the peak hourly demand rather than average daily use to avoid pressure drops during high-activity periods.

What maintenance and automation features are essential for long-term reliability?

Look for systems with PLC-based automated control and real-time monitoring of resistivity, temperature, and flow rates. Essential features include automatic chemical disinfection cycles, UV sterilization modules, and 0.22μm hydrophobic vent filters for storage tanks. A modular design is preferred to allow for easy replacement of membranes and resin canisters without total system downtime.

Cross-Border Procurement & Risk Management for Medical Equipment

What are the primary risks when importing medical water systems from overseas?

The biggest risks are regulatory non-compliance and damage during transit. Ensure the supplier provides a Certificate of Origin and Declaration of Conformity. Because these systems contain sensitive membranes and electronic controllers, specify vacuum-sealed moisture-proof packaging and reinforced wooden crate shielding to prevent vibration damage or salt-air corrosion during sea freight.

How should buyers negotiate technical support and after-sales service with international suppliers?

Negotiate for a comprehensive FAT (Factory Acceptance Test) via video link before shipping. Demand a 2-year warranty on core components (pumps and PLC) and ensure the supplier provides detailed English-language O&M manuals and installation videos. For complex systems, include a clause for remote technical diagnostics via 4G/Wi-Fi modules to allow the manufacturer to troubleshoot software issues from abroad.

What are the transaction security tips for high-value medical equipment orders?

Use secure payment methods such as Letter of Credit (L/C) or Escrow services provided by reputable platforms like Made-in-China.com. Never pay the full amount upfront; a standard structure is 30% deposit, 60% after FAT/before shipment, and 10% after successful installation and commissioning. Verify the supplier's Audited Supplier status to ensure they have a physical factory and valid business license.

What logistics and customs considerations apply to shipping to specific regions?

Medical systems are often classified under HS Code 842121. Check for specific import permits required by your local Ministry of Health. For shipping, FOB (Free On Board) is recommended if you have a reliable freight forwarder who understands medical device handling. Ensure all pressure vessels within the system have the necessary ASME or PED certifications to pass customs inspections without seizure.

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