“Standard” and custom programmes for every need. he equipment process is developed by our Automation Department, according to the current codes/standards and the type of product being processed. Vacuum breaker or pressure leak tests; load conditioning programme; vacuum sterilisation programme; product degassing programme; and a gas neutralising programme, etc. The ETO gas is injected at a temperature of 60°C into the chamber via a PID-controlled modulating valve and the condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during the entire sterilisation phase (temperature deviation below ± 1°C).
- Double-walled square 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 stainless steel with sanitary
- fittings (tri-clamp ferrules and hygienic flanges).
- Any surfaces that come into contact with the product and process fluids are mechanically polished to a roughness level of less than 0.35 micron.
- Automatic horizontal sliding chamber doors.
- Pneumatically pressurised chamber door sealing gasket (cwith process air).
- 316L/316Ti 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.
- Built-in steam generator.
- Built-in vacuum pump with a water recirculation system (water-saving system).
- Built-in ETO gas evaporation system.
- Built-in load conditioning, sterilising and degassing devices.
- Manual or fully automated ergonomic product loading and unloading solutions.
- Gas neutralisation system by means of a thermal combustor or scrubber.
- Floor or elevated loading solutions.
cGMP ethylene oxide sterilisers
PHARMA DIVISION
cGMP ethylene oxide sterilisers
The ETO sterilisers have been designed to sterilise – by means of ethylene oxide – heat-sensitive materials, such as plastic syringes, infusion sets, dialysis filter cartridges, plastic materials and special surgical tools.
POROUS AND NON-POROUS
ETHYLENE OXIDE + NITROGEN
20°C – 50°C
“Standard” and custom programmes for every need. he equipment process is developed by our Automation Department, according to the current codes/standards and the type of product being processed. Vacuum breaker or pressure leak tests; load conditioning programme; vacuum sterilisation programme; product degassing programme; and a gas neutralising programme, etc. The ETO gas is injected at a temperature of 60°C into the chamber via a PID-controlled modulating valve and the condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during the entire sterilisation phase (temperature deviation below ± 1°C).
- Double-walled square 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 stainless steel with sanitary
- fittings (tri-clamp ferrules and hygienic flanges).
- Any surfaces that come into contact with the product and process fluids are mechanically polished to a roughness level of less than 0.35 micron.
- Automatic horizontal sliding chamber doors.
- Pneumatically pressurised chamber door sealing gasket (cwith process air).
- 316L/316Ti 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.
- Built-in steam generator.
- Built-in vacuum pump with a water recirculation system (water-saving system).
- Built-in ETO gas evaporation system.
- Built-in load conditioning, sterilising and degassing devices.
- Manual or fully automated ergonomic product loading and unloading solutions.
- Gas neutralisation system by means of a thermal combustor or scrubber.
- Floor or elevated loading solutions.
cGMP ethylene oxide sterilisers
PHARMA DIVISION
cGMP ethylene oxide sterilisers
The ETO sterilisers have been designed to sterilise – by means of ethylene oxide – heat-sensitive materials, such as plastic syringes, infusion sets, dialysis filter cartridges, plastic materials and special surgical tools.
POROUS AND NON-POROUS
ETHYLENE OXIDE + NITROGEN
20°C – 50°C
cGMP ethylene oxide sterilisers
PHARMA DIVISION
cGMP ethylene oxide sterilisers
The ETO sterilisers have been designed to sterilise – by means of ethylene oxide – heat-sensitive materials, such as plastic syringes, infusion sets, dialysis filter cartridges, plastic materials and special surgical tools.
POROUS AND NON-POROUS
ETHYLENE OXIDE + NITROGEN
20°C – 50°C
“Standard” and custom programmes for every need. he equipment process is developed by our Automation Department, according to the current codes/standards and the type of product being processed. Vacuum breaker or pressure leak tests; load conditioning programme; vacuum sterilisation programme; product degassing programme; and a gas neutralising programme, etc. The ETO gas is injected at a temperature of 60°C into the chamber via a PID-controlled modulating valve and the condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during the entire sterilisation phase (temperature deviation below ± 1°C).
- Double-walled square 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 stainless steel with sanitary
- fittings (tri-clamp ferrules and hygienic flanges).
- Any surfaces that come into contact with the product and process fluids are mechanically polished to a roughness level of less than 0.35 micron.
- Automatic horizontal sliding chamber doors.
- Pneumatically pressurised chamber door sealing gasket (cwith process air).
- 316L/316Ti 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.
- Built-in steam generator.
- Built-in vacuum pump with a water recirculation system (water-saving system).
- Built-in ETO gas evaporation system.
- Built-in load conditioning, sterilising and degassing devices.
- Manual or fully automated ergonomic product loading and unloading solutions.
- Gas neutralisation system by means of a thermal combustor or scrubber.
- Floor or elevated loading solutions.
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