4.4 Sterilisation program specifications
Cycle name
Cycle type
Sterilisation temperature
Sterilisation pressure
Sterilisation phase duration
Minimum drying phase duration
Average total cycle duration
Average H
0 consumption
2
Average energy consumption
4.5 Putting the material to be sterilised in the chamber
Package the load very carefully, making sure that the medical devices are compatible with the chosen packaging.
The chosen packaging material must be:
- Compatible with the sterilisation process.
- Compatible with the labelling system.
Only use medical packaging that is compliant with: EN 868-5 and ISO 11607-1 qualified for 134°C cycles.
To check that the thermodynamic sterilisation cycle has completed successfully, always put a class 5 chemical indicator in together with the
load in accordance with ISO 11140-1. Choose the indicator according to the selected cycle (121°C or 134°C)
Place the clean material on the trays and distribute them evenly.
The chamber can contain a maximum of:
Unpacked
solid material
HC 40
HC 40 Plus
Objects in bags must be placed on the trays with the transparent part of the package facing down.
4.5.1 Preparing the material
First of all, remember that when handling and moving contaminated
material, it is good practice to take the following precautions:
- Wear suitably thick rubber gloves and a face mask;
- Wash your already-gloved hands with a germicidal detergent;
- Always use a tray to transport instruments.
- Never transport then directly in your hand;
- To avoid the risk of contracting hazardous infections, protect you
hands from contact with any sharp or pointed parts;
- Immediately separate any items that must not be sterilised or that
cannot support the process;
- When you have finished handling the unsterile material, wash your
still-gloved hands thoroughly. All materials and/or instruments to
be sterilised must be perfectly clean and free of any kind of residue
(organic/inorganic deposits, paper fragments, cotton/gauze pads,
limescale, etc.).
NOTE
In addition to causing problems during the sterilisation process,
failure to clean and remove residues can damage the instruments
and/or the steriliser.
134 STD
134°C
316 kPa
4 min
16 min
17 litres
43 min
22 litres
47 min
17 litres
415 ml
22 litres
455 ml
17 litres
515 Wh
22 litres
646 Wh
Standard Cycles
Packed
solid material
5,5 kg
3,5 kg
6,5 kg
4 kg
Sterilisation cycles type B
121 STD
134 Prion 134 B- Flash
B
121°C
134°C
214kPa
316 kPa
16 min
18 min
16 min
16 min
54 min
57 min
57 min
59 min
455 ml
510 ml
500 ml
540 ml
547 Wh
598 Wh
654 Wh
706 Wh
B Cycles
134 B- Flash Cycles
Porous
Packed
load
solid material
1,5 kg
0,5 kg
2 kg
0,7 kg
NOTE
In addition to causing problems during the sterilisation
process, failure to clean and remove residues can damage
the instruments and/or the steriliser.
Proceed as described to clean effectively:
1. Rinse the instruments under a jet of running water immediately
after use;
2. Separate metal instruments by material type (carbon steel,
stainless steel, brass, aluminium, chromium, etc.) to prevent
electrolytic oxidisation;
3. Wash with an ultrasonic cleaner containing a mixture of water
and germicidal solution, carefully following the manufacturers
recommendations. Alternatively, use a thermal disinfector.
4. For better results, use a detergent specifically for ultrasonic
cleaning, with a neutral pH.
NOTE
Solutions that contain phenol or quaternary ammonium
based compounds can corrode the instruments and the
metal parts of the ultrasonic equipment.
5. After washing, rinse the instruments thoroughly and check that
the residues have been completely removed. Repeat the washing
cycle or wash by hand if necessary.
Sterilisation cycles typ S
134
Universal S
S
134°C
134°C
316 kPa
316 kPa
3,5 min
3,5 min
6 min
16 min
32 min
36 min
32 min
37 min
300 ml
260 ml
315 ml
275 ml
390 Wh
375 Wh
425 Wh
450 Wh
S Cycles
Porous
Packed
load
solid material
0,2 kg
2,5 kg
0,3 kg
3,0 kg
121
Softprogr.
121°C
214kPa
15,5 min
16 min
47 min
EN
48 min
295 ml
300 ml
410 Wh
480 Wh
Porous
load
0,3 kg
0,4 kg
57