Sanitary Hydranautics
SanRO® elements are USP (United States Pharmacopoeia)-compliant and are typically used in producing purified water in pharmaceutical, medical, biotechnology, food, beverage, and semiconductor processes. Elements meet all requirements for purified water (PW) and conform to FDA Regulation CFR, Title 21. Hydranautics SanRO® elements feature a net-type outer wrapping that allows easy access for cleaning in place, reducing the potential for element fouling and residual accumulation of contaminants on the element’s exterior. Sites where microbial growth might occur are thereby eliminated when compared with fiberglass-wrapped elements. Heat sanitization reaches areas where biocides may not be able to reach and is also a process that is easy to monitor and control.
Membranes for high performance USP water purification systems. Elements conform to FDA Regulation CFR, Title 21 and are used for operating temperatures up to 45°C.
| Model No. | Flow Rate* | Pressure Rating (PSI) | Nominal Salt Rejection | Size* (Dia. x L) |
|
| (GPD) | (m3/d) | ||||
| SanROO HS-4 | 2,200 | 8.3 | 225 | 99.7 | 4″ x 40″ |
| SanRO HS2-4 | 3,000 | 11.4 | 225 | 99.6 | 4″ x 40″ |
| SanRO HS-8 | 8,800 | 33.3 | 225 | 99.7 | 8″ x 40″ |
| SanRO HS2-8 | 14,000 | 53.0 | 225 | 99.6 | 8″ x 40″ |
Please see product specification sheets for the test conditions under which the stated performance are based, and exact membrane element dimensions.
- Conforms to FDA Regulation CFR, Title 21
- Reduced bacteria growth potential by eliminating “dead” flow areas.
- Produces USP Classified Water
- Specially selected components for durability in daily sanitization
- Largest possible active membrane area for high flux and low energy costs
- Energy-saving, highly permeable, high rejection membrane
- All elements are heat-set at factory for predictable flows at outset of installation
- 100% of elements are wet-tested to ensure performance accountability, traceability, and adherence to flow and rejection standards
- ISO 9001-compliant manufacturing
- Computerized application design provided by Hydranautics’ IMSDesign software program
- Conformance with CGMPs
- Reduction of bacterial endotoxins and microbes
- Opthalmic and inhalation product production
- Reduction of TDS, TOC and colloids from high purity water
- Removal of algae, fungi, mold, yeast and bacteria as measured in “colony forming units” (CFU)
- Removal of bacteria from cell walls of polysaccharide compounds which can cause fever, shock or death as measured in “endotoxin units” (EU/ml)
- Reduction of microbial growth by minimizing nutrients
- Electronics-grade ultrapure water
- Water for cosmetic production
- Nutriceutical production
- Food and beverage production
- Container rinsing
- Production of ultrapure or PW (Purified Water) for the cleaning of fermentation equipment and dialysis machines and WFI (water for injection).
- Wine de-alcoholization
- Replacement of distillation systems, providing lower energy usage and costs