Predefined and “custom” programmes for every need. The equipment process is developed by our Automation Department, according to the current regulations/standards and the type of product being sterilised. Sterilisation chamber pressure or vacuum tests; Bowie & Dick tests; Helix tests; automatic filter breaker test with integrity tests; solid component and porous load programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; programme for liquids in syringes; sensitive/fragile product (e.g. filter cartridges) programme; rubber cap programme; decontamination cycle with chamber condensate sterilisation and drain filtration, in compliance with BSL3 and BSL4, etc. The steam is injected into the sterilisation chamber via a PID-controlled automatic modulating valve and the generated condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during all the sterilisation phases (temperature deviation below ± 0.4°C).
- Circular, quadrangular or rectangular sterilisation chamber with quadrangular or rectangular hatches (doors).
- An ashlar-type cavity completely envelopes the chamber to quickly and uniformly heat/cool the loads.
- Fully welded one-piece chamber with rounded corners to ensure excellent hygiene levels and facilitate internal surface cleaning.
- The mechanical construction is resistant to temperatures above 140°C.
- Some reinforcements are welded onto the outside of the cavity to ensure stability during operating conditions.
- The chamber is positioned on a tubular-type base to evenly distribute the weight on the floor.
- The loading trolley-inserting and removing guides are positioned on the bottom of the chamber; they are also height-adjustable.
- Two 1.5” tri-clamp ferrules are welded to the chamber for validation purposes (temperature uniformity mapping and pressure tests).
- All of the chambers internal surfaces are mechanically polished and then subjected to chemical degreasing, pickling and passivation treatments. Surface finish: ≤ 0.35 micron.
- The bottom of the chamber converges towards the drain sump in order to make disposing of the condensate easier.
- Above-floor or recessed chamber installation possible (depending on the size).
- Both doors (loading and pick-up side) have been designed to be connected to the walls of the clean chambers (“Bio-seal” interface).
cGMP saturated steam autoclaves
PHARMA DIVISION
cGMP saturated steam autoclave description
The RSA Autoclaves have been designed to sterilise – by means of clean saturated steam – heat-resistant and moisture-stable materials, such as metal parts, plastic or rubber components, liquids in ventilated (open) or sealed (hermetically) containers, filter cartridges and clothing, etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
Predefined and “custom” programmes for every need. The equipment process is developed by our Automation Department, according to the current regulations/standards and the type of product being sterilised. Sterilisation chamber pressure or vacuum tests; Bowie & Dick tests; Helix tests; automatic filter breaker test with integrity tests; solid component and porous load programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; programme for liquids in syringes; sensitive/fragile product (e.g. filter cartridges) programme; rubber cap programme; decontamination cycle with chamber condensate sterilisation and drain filtration, in compliance with BSL3 and BSL4, etc. The steam is injected into the sterilisation chamber via a PID-controlled automatic modulating valve and the generated condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during all the sterilisation phases (temperature deviation below ± 0.4°C).
- Circular, quadrangular or rectangular sterilisation chamber with quadrangular or rectangular hatches (doors).
- An ashlar-type cavity completely envelopes the chamber to quickly and uniformly heat/cool the loads.
- Fully welded one-piece chamber with rounded corners to ensure excellent hygiene levels and facilitate internal surface cleaning.
- The mechanical construction is resistant to temperatures above 140°C.
- Some reinforcements are welded onto the outside of the cavity to ensure stability during operating conditions.
- The chamber is positioned on a tubular-type base to evenly distribute the weight on the floor.
- The loading trolley-inserting and removing guides are positioned on the bottom of the chamber; they are also height-adjustable.
- Two 1.5” tri-clamp ferrules are welded to the chamber for validation purposes (temperature uniformity mapping and pressure tests).
- All of the chambers internal surfaces are mechanically polished and then subjected to chemical degreasing, pickling and passivation treatments. Surface finish: ≤ 0.35 micron.
- The bottom of the chamber converges towards the drain sump in order to make disposing of the condensate easier.
- Above-floor or recessed chamber installation possible (depending on the size).
- Both doors (loading and pick-up side) have been designed to be connected to the walls of the clean chambers (“Bio-seal” interface).
cGMP saturated steam autoclaves
PHARMA DIVISION
cGMP saturated steam autoclave description
The RSA Autoclaves have been designed to sterilise – by means of clean saturated steam – heat-resistant and moisture-stable materials, such as metal parts, plastic or rubber components, liquids in ventilated (open) or sealed (hermetically) containers, filter cartridges and clothing, etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
cGMP saturated steam autoclaves
PHARMA DIVISION
cGMP saturated steam autoclave description
The RSA Autoclaves have been designed to sterilise – by means of clean saturated steam – heat-resistant and moisture-stable materials, such as metal parts, plastic or rubber components, liquids in ventilated (open) or sealed (hermetically) containers, filter cartridges and clothing, etc.
POROUS, NON-POROUS AND LIQUIDS
SATURATED STEAM
121°C – 134°C
Predefined and “custom” programmes for every need. The equipment process is developed by our Automation Department, according to the current regulations/standards and the type of product being sterilised. Sterilisation chamber pressure or vacuum tests; Bowie & Dick tests; Helix tests; automatic filter breaker test with integrity tests; solid component and porous load programme; programme for liquids in ventilated containers; programme for liquids in sealed containers; programme for liquids in syringes; sensitive/fragile product (e.g. filter cartridges) programme; rubber cap programme; decontamination cycle with chamber condensate sterilisation and drain filtration, in compliance with BSL3 and BSL4, etc. The steam is injected into the sterilisation chamber via a PID-controlled automatic modulating valve and the generated condensate is continuously evacuated through the drain, in order to ensure excellent heat distribution during all the sterilisation phases (temperature deviation below ± 0.4°C).
- Circular, quadrangular or rectangular sterilisation chamber with quadrangular or rectangular hatches (doors).
- An ashlar-type cavity completely envelopes the chamber to quickly and uniformly heat/cool the loads.
- Fully welded one-piece chamber with rounded corners to ensure excellent hygiene levels and facilitate internal surface cleaning.
- The mechanical construction is resistant to temperatures above 140°C.
- Some reinforcements are welded onto the outside of the cavity to ensure stability during operating conditions.
- The chamber is positioned on a tubular-type base to evenly distribute the weight on the floor.
- The loading trolley-inserting and removing guides are positioned on the bottom of the chamber; they are also height-adjustable.
- Two 1.5” tri-clamp ferrules are welded to the chamber for validation purposes (temperature uniformity mapping and pressure tests).
- All of the chambers internal surfaces are mechanically polished and then subjected to chemical degreasing, pickling and passivation treatments. Surface finish: ≤ 0.35 micron.
- The bottom of the chamber converges towards the drain sump in order to make disposing of the condensate easier.
- Above-floor or recessed chamber installation possible (depending on the size).
- Both doors (loading and pick-up side) have been designed to be connected to the walls of the clean chambers (“Bio-seal” interface).
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