Process Filtration
Filtration support for process lines and production workflows.
Dairy ProcessingPasteurizers, CIP systems, transfer lines
Food ProcessingSanitary fittings, valves and tubing
Beverage LinesBottling, mixing and hygienic transfer
PharmaceuticalHigh-purity 316L and documentation
BiotechnologyBioreactors, skids and cell culture support
OEM / ContractorsProject RFQ support and secondary supply
Process Equipment
Filtration and separation equipment RFQs depend on media, flow, housing, filtration target, material and documentation requirements.
Applications
Filtration and separation requirements should be defined with media, target, flow and service conditions.
Filtration support for process lines and production workflows.
Documentation-driven filtration inquiry support.
Industrial process separation support by RFQ.
Sizes & Dimensions
Single and multi-element housings sized for various flow rates and micron ratings. Tri-clamp inlet/outlet standard.
| Housing | Element | Qty | Flow (L/min) | Inlet/Outlet | Material |
|---|---|---|---|---|---|
| Single 10" | 10" | 1 | 40 – 80 | ¾" Tri-Clamp | 316L |
| Single 20" | 20" | 1 | 80 – 160 | 1" Tri-Clamp | 316L |
| Single 30" | 30" | 1 | 120 – 240 | 1½" Tri-Clamp | 316L |
| Multi 3×10" | 10" | 3 | 120 – 240 | 1½" Tri-Clamp | 316L |
| Multi 5×20" | 20" | 5 | 400 – 800 | 2" Tri-Clamp | 316L |
| Multi 7×30" | 30" | 7 | 840 – 1680 | 3" Tri-Clamp | 316L |
| Bag P1 | 17" | 1 | 120 – 240 | 1½" Tri-Clamp | 316L |
| Bag P2 | 32" | 1 | 240 – 480 | 2" Tri-Clamp | 316L |
Operating Conditions
Housing pressure rated to 10 bar. Maximum differential pressure across element 2.5 bar before replacement.
Actual ratings depend on size, material and operating conditions. Confirm via RFQ for project-specific requirements.
Standards & Compliance
Full documentation packages available including MTR, 3.1 certificates, surface roughness reports and pressure test records.
Sanitary equipment for milk and milk products processing.
Surface finish, materials and design for pharma/biotech.
European hygienic engineering and design certification.
Construction code for pressure vessels.
Food contact materials compliance for seats and seals.
USP biological reactivity testing for plastics.
Product Variants
Multiple variants available to match your application requirements. Browse related products for complete process line coverage.


Bag filter vessels for higher dirt-holding capacity at lower cost.
Request quote →

Technical Overview
Selection depends on media, flow, filtration target and system design.
| Requirement | Typical Information Needed |
|---|---|
| Product Type | Filtration or separation equipment |
| Material Grade | 304 / 316L stainless steel by RFQ |
| Flow / Media | Flow rate, media and target separation |
| Connection | Process inlet/outlet and utility interfaces |
| Documentation | Drawings, certificates and inspection by RFQ |
Include media, flow, target filtration, material, connection, quantity and documentation expectations.
Material certificates, finish notes, inspection requirements, heat traceability and supplier documentation can be included in the quotation package.
Send media, flow, filtration target, material and documentation needs.
Common Questions
Engineering and procurement questions we hear most often. For project-specific guidance, send your application details via RFQ.
For sterile filtration (bacteria removal): 0.22 μm. Mycoplasma: 0.1 μm. Polishing: 0.45 μm. Coarse: 1-25 μm. Strainers: 100+ μm.
Provide media specifications (particle size distribution) for filter selection. Sterile applications require absolute-rated filters.
Depends on dirt loading. Track differential pressure (ΔP). Replace when ΔP exceeds 2.0-2.5 bar (housing max).
For sterile filtration in bioprocess, integrity test each cartridge before/after use. Document with batch records.
Integrity testing verifies sterile filter is intact before/after use. Methods: bubble point, diffusion flow, water intrusion.
Required for sterile pharmaceutical applications. Document each test. Failed test = batch rejection. Specify automated integrity tester with system.
Yes — sanitary filter housings are SIP-rated for +135°C steam. Element compatibility varies — verify with cartridge manufacturer.
For frequent SIP, specify steam-rated cartridges (PTFE-membrane) and PTFE gaskets. Standard polypropylene cartridges have limited SIP life.
Bag filters: higher dirt capacity, lower cost per gram of dirt, easier disposal. Cartridges: better filtration efficiency, integrity-testable.
For prefiltration or coarse: bags economical. For sterile or critical: cartridges required. Often combined: bag → cartridge sequence.
Standard: 3.1 MTR for housing, FDA compliance for gaskets, pressure test certificate, dimensional drawing.
For pharma: full BPE package, USP Class VI for elastomers, helium leak test. Cartridge documentation separate (from cartridge supplier).
Yes — complete filtration skids available with pumps, controls, automatic backwash, and integrity test capability.
Provide flow rate, micron rating, integrity test requirements, and automation level. Skid sized to flow and pressure requirements.