• Double-walled square or rectangular chamber, made entirely from 316L or 316Ti stainless steel.
  • Ashlar-type total cavity comprising 304 or 316L/316Ti stainless steel.
  • Piping made entirely from 316L or 304 stainless steel.
  • Any surfaces that come into contact with the product and process fluids are mechanically satin-finished to a roughness level of less than 1 micron.
  • Manual folding chamber doors or vertical/horizontal automatic sliding doors.
  • Pneumatically pressurised chamber door sealing gasket (with process air).
  • 316L/316Ti/304 stainless steel components and tools, in addition to elastomers manufactured in compliance with FDA 21 CFR, Part 177.
  • The chamber, heads, pipes, components and instruments are properly insulated by a cutting-edge material.
  • Zone separation by means of a 304 or 316L/316Ti stainless steel “bio-seal” septum (BSL 3 and BSL 4).
  • “Bio-seal” flange to connect to the VHP isolator.
  • Manual or fully automated ergonomic product loading and unloading solutions.
  • Floor or elevated loading solutions.