Sterilizing-Grade & Depth Filtration — Food/Beverage/Biological Process Fluids
Named chemicals
What LibertyCES's vendor documentation shows
Strainrite's compliance stack is the content: ISO 9001:2015, cGMP manufacturing in validated ISO Class 7 clean rooms, USP Class VI biological reactivity, LAL endotoxin testing, bacterial challenge validation to ASTM F838, FDA-listed materials, steam and gamma sterilization validation, every cartridge individually integrity-tested via air diffusion test. Endo-MAXX CN's zeta-potential mechanism is genuinely differentiated — it removes charged particles SMALLER than its own absolute rating, which nothing else in the corpus does. Commercial angle: the vendor cites domestic US manufacturing specifically to avoid the 6-12 month delivery delays it says competitors face.
Materials documented for this service
- PES membrane (0.2µm sterilizing grade)
- Hydrophobic PTFE, double-layer (Vent-MAXX)
- Charged nylon (Endo-MAXX CN)
- Ultrapure polypropylene (capsules)
- FDA-listed materials of construction
Products cited for this service
Sourced to
- data/vendor-sources/allied-fluid-products-line-card.md
Every material and product claim on this page traces to the vendor documentation listed above. Chemical compatibility depends on exact concentration, temperature, and duty cycle — confirm current specifications with the manufacturer and request a spec review before final specification.