“Standard” and custom programmes for every need. The equipment process is developed by our Automation Department, according to the current codes/standards and the type of product to be processed. Vacuum breaker tests; Bowie & Dick tests; Helix tests; air filter in situ sterilisation and integrity tests; solid and porous material programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; highly-sensitive material (filters) programme; rubber cap programme; Decontamination cycle in compliance with BSL3 and BSL4 etc. The steam is injected 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 ± 0.4°C).
- 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.
cGLP steam autoclaves
LAB DIVISION
Steam Autoclave Description
The NEBULA autoclaves have been designed to sterilise heat-resistant and moisture-stable materials – such as metal parts, plastic and rubber components, liquids in ventilated or sealed containers, and fabrics etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
“Standard” and custom programmes for every need. The equipment process is developed by our Automation Department, according to the current codes/standards and the type of product to be processed. Vacuum breaker tests; Bowie & Dick tests; Helix tests; air filter in situ sterilisation and integrity tests; solid and porous material programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; highly-sensitive material (filters) programme; rubber cap programme; Decontamination cycle in compliance with BSL3 and BSL4 etc. The steam is injected 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 ± 0.4°C).
- 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.
cGLP steam autoclaves
LAB DIVISION
Steam Autoclave Description
The NEBULA autoclaves have been designed to sterilise heat-resistant and moisture-stable materials – such as metal parts, plastic and rubber components, liquids in ventilated or sealed containers, and fabrics etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
cGLP steam autoclaves
LAB DIVISION
Steam Autoclave Description
The NEBULA autoclaves have been designed to sterilise heat-resistant and moisture-stable materials – such as metal parts, plastic and rubber components, liquids in ventilated or sealed containers, and fabrics etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
“Standard” and custom programmes for every need. The equipment process is developed by our Automation Department, according to the current codes/standards and the type of product to be processed. Vacuum breaker tests; Bowie & Dick tests; Helix tests; air filter in situ sterilisation and integrity tests; solid and porous material programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; highly-sensitive material (filters) programme; rubber cap programme; Decontamination cycle in compliance with BSL3 and BSL4 etc. The steam is injected 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 ± 0.4°C).
- 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.
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