Process notes for ordering.
Pharmaceutical and fine chemical filtration often combines validated micron retention, chemical compatibility and documentation packages — values below support technical quotation only. Retention test method, extractables concern and FAI criteria must be agreed per project before production release and shipment.
| Parameter | Typical range (pharma / chemical) | Notes for RFQ |
|---|---|---|
| Fluid | Solvents; API intermediates; WFI support | Full chemical name; concentration; temperature |
| Retention | Approx. 2–40 μm nominal common | Absolute vs nominal; test method if required |
| Temperature | Ambient to 150 °C+ (duty-dependent) | Peak and CIP temperature |
| Pressure / ΔP | Housing-limited | Share max allowable differential pressure |
| Cleaning | Solvent flush; CIP; steam (if used) | Affects media and seal selection |
| Validation | FAI; lot trace; test reports | Define on PO before lead time lock |
Operating limits vary by equipment — values confirmed per project.
For sintered discs and cartridges, send drawing with tolerance bands and end-cap detail. For solvent duty, list extractables concern and maximum soak time. Validation documents and lot traceability scope are agreed before lead time is locked. MOQ confirmed after specification review.
Operating limits vary by equipment — values above are typical ranges, confirmed per project.
