Introduction
Eliminating Endotoxin Ultrapure Water System offers uninterrupted supply at rate of 38L/hour. Effectively removes RNases and DNases, ensuring contamination-free results for molecular research. Designed to achieve superior ion rejection and eliminate organic matter, enhancing purity. Endotoxin filtration technology supports critical biomedical and pharmaceutical applications. compact build optimizes space while maintaining performance efficiency.
Manufactured under strict quality control processes, complying with international laboratory equipment standards. Provides 1-year warranty for main components and lifetime technical support.
Applications
Eliminating Endotoxin Ultrapure Water System is ideal for research, diagnostics, and manufacturing processes in laboratories, pharmaceuticals, biotechnology, electronics, and healthcare industries.
Specifications
| Output | 38L/hour |
| Flowrate | 2L/min |
| Outlets | RO and UP |
| Feed Water | Portable tap water, 5 to 45℃, 1 to 4 bar |
| RO Water Quality | Ion rejection rate: greater than 98%, Organic rejection rate (MW above 200 daltons): greater than 99%, Particle and bacteria rejection rate: greater than 99% |
| UP Water Quality | Resistivity: greater than 18.2MΩ.cm at 25℃, Bacteria: less than 0.01CFU/ml, Particles (0.2µm): less than 1/ml, Heavy metal ion: less than 0.01ppb, Total organic carbon: less than 10ppb |
| Endotoxin | Less than 0.001EU/ml |
| RNases | Less than 1pg/ml |
| DNases | Less than 5pg/ml |
| Display | LCD |
| Power Consumption | 72W |
| Power Supply | AC100 to 240V, 50/60Hz |
| Dimension (L×B×H) | 340×500×560mm |
| Weight | 18Kg |
Features
Comprehensive system management functions
Multiple alarm option
Backlit LCD display
Two-way quality monitoring
Self-flushing RO membrane
Standard Accessories
Accessory | Unit | Quantity |
Cartridges | Set | 1 |
12L Pressure Tank | Each | 1 |
Accessory Bag | Pack | 1 |
FAQs
1. What is an Eliminating Endotoxin Ultrapure Water System?
An Eliminating Endotoxin Ultrapure Water System is a water purification apparatus designed to remove endotoxins and produce ultrapure water.
2. How does Eliminating Endotoxin Ultrapure Water System remove endotoxins?
It removes endotoxins using a combination of ultrafiltration, reverse osmosis, UV oxidation, and activated carbon filtration to achieve ultrapure water quality.
3. How does Eliminating Endotoxin Ultrapure Water System support cell culture research?
It supports cell culture research by providing water free of pyrogens, which can otherwise disrupt cell growth and experimental outcomes.
4. How does Eliminating Endotoxin Ultrapure Water System improve biopharmaceutical quality control?
It improves biopharmaceutical quality control by supplying ultrapure water that meets stringent endotoxin limits for batch testing and formulation.
5. How is Eliminating Endotoxin Ultrapure Water System used in vaccine production?
It is used in vaccine production to prevent endotoxin contamination that could compromise vaccine safety and efficacy.
6. What is the role of Eliminating Endotoxin Ultrapure Water System in gene therapy manufacturing?
It plays a key role in gene therapy manufacturing by ensuring the purity of vectors and reagents used in sensitive genetic modification processes.
7. How does Eliminating Endotoxin Ultrapure Water System contribute to sterile filtration processes?
It contributes to sterile filtration processes by supplying ultra-clean water that prevents filter fouling and ensures process integrity.
8. Can Eliminating Endotoxin Ultrapure Water System be used in microfluidics research?
It is ideal for microfluidics research where even trace endotoxins can alter flow characteristics or affect biochemical reactions.
9. Can Eliminating Endotoxin Ultrapure Water System be used in forensic laboratories?
It is used in forensic laboratories to eliminate any water-based contamination that could compromise DNA evidence integrity.
10. Can Eliminating Endotoxin Ultrapure Water System be used in cytotoxic drug compounding?
It is used in cytotoxic drug compounding to prevent contamination that could compromise drug stability and safety.
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