Operating Instructions
52 Pages
Preview
Page 1
Operating Instructions
ATMOS S 351 NATAL English
0124
GA1GB.210302.0 2020-06 Index 01
E349855
Table of contents 1 1.1 1.2 1.3 1.4 1.5 1.6 1.7
Introduction...4 Notes on operating instructions...4 Explanation of pictures and symbols...5 Intended use...7 Function...9 Intended users...9 Scope of delivery... 10 Transport and storage... 11
2 2.1 2.2 2.3
Notes for your safety...12 General safety instructions... 12 Danger for users, patients and third parties... 12 Avoiding damage to the device... 14
3 Setting up and starting up...16 3.1 Device overview... 16 3.1.1 Secretion canister... 17 3.2 Preparing the device... 18 3.3 Connecting to the mains power supply... 18 3.4 Connecting the secretion canister system and hoses... 19 4 Operation...20 4.1 Ambient conditions during operation... 20 4.2 Control panel... 20 4.3 Switching on the device... 20 4.4 Switching off the device... 21 4.5 Explanation of the display... 21 4.6 Vacuum extraction mode... 21 4.7 User menu... 22 4.7.1 Language... 22 4.7.2 Vacuum unit... 22 4.7.3 Vacuum extraction... 23 4.7.4 Brightness... 24 4.7.5 Date... 24 4.7.6 Time... 24 4.7.7 Vacuum steps... 25 4.8 Vacuum extraction... 25 4.8.1 Additional functions... 26 4.8.2 Vacuum drop during vacuum build-up... 26 4.8.3 Vacuum drop after final vacuum has been reached... 26 4.8.4 Final vacuum is not reached... 27 4.9 Suction... 27 4.10 Electronic fill-level monitoring system... 27 4.11 Changing the secretion canister... 28 4.12 Warning messages... 28 4.13 Trolley for ATMOS S 351 with standard rail (REF 320.0070.0)... 29 4.14 Trolley for ATMOS S 351 (REF 444.0020.0)... 29 4.15 Foot controller... 30 4.16 Checking the bacterial filter... 30
2
5 Reprocessing...31 5.1 Safety instructions for reprocessing... 31 5.1.1 General safety instructions... 31 5.1.2 Danger for users, patients and third parties... 31 5.1.3 Avoiding damage to the device... 31 5.2 Preparing and completing reprocessing... 32 5.3 Preparing surfaces... 32 5.3.1 Overview... 32 5.3.2 Selecting process chemicals... 33 5.3.3 Wipe cleaning... 34 5.3.4 Wipe disinfection... 34 5.4 Reprocessing the accessories... 34 5.4.1 Overview... 34 5.4.2 Selecting process chemicals... 34 5.4.3 Secretion canister system... 35 5.4.4 Hoses... 36 6 Maintenance and service...38 6.1 Periodic tests... 38 6.2 Function check ... 38 6.2.1 Visual inspection... 38 6.2.2 Function test... 39 6.2.3 Monitoring... 40 6.3 Sending in the device... 41 7
Troubleshooting...42
8
Accessories...44
9
Consumables...45
10
Disposal...46
11
Technical data...47
12
Notes on EMC...49
13
Notice...50
14
Notice...51
3
1
Introduction
1.1
Notes on operating instructions These operating instructions contain important instructions on how to operate your product safely, correctly and effectively. These operating instructions are designed for training and instructing new operating personnel in the use of the system, and they are also intended for use as a reference manual. This document may only be reprinted, either in part or in whole, with written permission from ATMOS. These operating instructions must always be kept available near the product. Care, periodic tests, regular cleaning and proper application are essential. They ensure the operational safety and usability of the product. Maintenance, repairs and periodic tests may only be carried out by persons who have the appropriate technical knowledge and who are familiar with the product. The person must possess the test devices and original spare parts required to carry out these measures. Read chapter „2 Notes for your safety“ on page 12 before using the product for the first time. This will help you to avoid potentially dangerous situations. The product bears the CE marking CE 0124 in accordance with EC Council Directive 93/42/EEC concerning medical devices and meets the basic requirements of Annex I to this directive. The product complies with all the applicable requirements of Directive 2011/65/EU on the restriction of the use of certain hazardous substances in electrical and electronic equipment (‘RoHS’). The Declarations of Conformity and our General Terms and Conditions can be viewed on our website at www.atmosmed.com. The quality management system at ATMOS has been certified according to international standard EN ISO 13485.
These operating instructions are valid for the following devices:
4
Introduction
ATMOS S 351 NATAL, 230 V
444.0401.0
ATMOS S 351 NATAL, 100 V
444.0401.1
ATMOS S 351 NATAL, 115 V
444.0401.2
ATMOS S 351 NATAL, 127 V
444.0401.3
ATMOS S 351 NATAL, 230 V
444.0491.0
ATMOS S 351 NATAL, 100 V
444.0491.1
ATMOS S 351 NATAL, 115 V
444.0491.2
ATMOS S 351 NATAL, 127 V
444.0491.3
ATMOS S 351 NATAL – basic set, 230 V
444.0490.0
ATMOS S 351 NATAL – basic set, 100 V
444.0490.1
ATMOS S 351 NATAL – basic set, 115 V
444.0490.2
ATMOS S 351 NATAL – basic set, 127 V
444.0490.3
ATMOS S 351 NATAL – basic set, 230 V (Medi-Vac®)
444.0492.0
ATMOS S 351 NATAL – basic set, 230 V (Serres®)
444.0493.0
ATMOS S 351 NATAL mobile, 230 V
444.0481.0
ATMOS S 351 NATAL mobile, 100 V
444.0481.1
ATMOS S 351 NATAL mobile, 115 V
444.0481.2
ATMOS S 351 NATAL mobile, 127 V
444.0481.3
ATMOS S 351 NATAL mobile with foot controller, 230 V
444.0482.0
ATMOS S 351 NATAL mobile with foot controller, 100 V
444.0482.1
ATMOS S 351 NATAL mobile with foot controller, 115 V
444.0482.2
ATMOS S 351 NATAL mobile with foot controller, 127 V
444.0482.3
1.2
Explanation of pictures and symbols
In the operating instructions DANGER Warning of a danger that will result in immediate fatal or serious injury. Observe the necessary measures. WARNING Warning of a danger that can cause fatal or serious injury. Observe the necessary measures. CAUTION Warning of a danger that can cause minor injury. Observe the necessary measures. ATTENTION Notice of a danger that can damage the product or other objects. Observe the necessary measures. Warning of a danger that can cause fatal or serious injury. Notice of potential material damage.
Useful information on the handling of the device.
1.
Action. Proceed step by step.
»
Result of an action. Move in this direction, plug in.
click
Engage, check correct fit.
On device and type plate
Follow operating instructions (blue) Observe the operating instructions
Introduction
5
Warning; pay special attention 0124
This product complies with the relevant requirements of EU Directives. This product complies with the relevant requirements of EU Directives. UL Listing Mark
E349855
MEDICAL - GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH ANSI/AAMI ES60601-1 (2005) + AMD 1 (2012) CAN/CSA-C22.2 No. 60601-1 (2014) IEC 60601-1-6 (2013) Eurasian conformity GOST Certificate (Russia) Manufacturer Manufacturing date
SN
Serial number
REF
Order number
EAN
European Article Number Applied part type B
IPX0
No protection from water Professional disposal For single use only (symbol located on consumables)
STERILE
AUTOCLAVE
PATIENT LATEX
6
Introduction
Product is sterile (unless packaging is damaged or opened) Autoclavable Connection for suction hose / patient (Serres® canister system) No natural rubber latex
Potential equalisation Fuse Starting the vacuum extraction mode Stopping the vacuum extraction mode
-
Reduce vacuum
+
Increase vacuum
MAX
Maximum vacuum
SEMI
Vacuum extraction mode ‘SEMI’ activated
AUTO
Vacuum extraction mode ‘AUTO’ activated
S
Seconds Connected with trolley Foot controller Fragile, handle with care Store in a dry place Protect from sunlight
1.3
Intended use
Product name:
ATMOS S 351 NATAL
Main function:
An electric suction pump controlled by a microprocessor generates negative pressure. Due to the controlled negative pressure, parts of the body, in particular the head of a baby, are fixed. The microprocessor allows the desired vacuum to be gently increased and decreased within the defined unit of time and enables a controlled shutdown of the pump. An additional secretion canister must be attached to allow for temporary collection of drained body fluids.
Introduction
7
Intended use / intend- Vacuum extraction, surgical suction (among others: suction ed purpose: curettage, suction biopsy), bronchial suction in newborns Intended user / user profile:
Medical staff (among others: gynaecologists, midwives)
Intended patient group:
Generally, female patients of child-bearing age with and without restrictions; newborns.
Disease state to be diagnosed, treated or monitored:
Inapplicable
Application organ:
Natural orifices as well as openings resulting from surgical procedures (entire body)
Application time:
Short-term use on the patient (< 60 minutes)
Area of application:
The area of application is the clinical setting (among others: OT and delivery room). The device may only be used by staff who have been medically trained and instructed.
Criteria for patient selection:
Patients who benefit from vacuum extraction, a surgical procedure or bronchial suction
Indications:
• For vacuum extraction • In surgical procedures (e.g. suction curettage, suction biopsy) • For bronchial suction in newborns
Medical contraindica- Not suitable for: tions: • Continuous operation for drainage procedures in the low vacuum range (e.g. cardiothoracic or wound drainage) • Smoke evacuation • Liposuction • Emergency and rescue use Other contraindications:
8
Introduction
• No application outside of medical areas • No suction of flammable, corrosive or explosive fluids/ gases
Warning notes:
The following complications can occur during vacuum extraction or suction: • Cerebral haemorrhages • Cephalohaematomas • Skin abrasions on the child’s head • Haematomas • Perineal, vaginal, cervical tears • Bleeding • Injuries to vessels and nerves • Adhesion of the suction instrument
The product is:
Active
Sterility / specific microbial condition:
Not a sterile product
Single-use product / reprocessing:
The device and parts of the accessories are reusable. For information on reprocessing, cleaning and disinfection, please see the operating instructions.
1.4
Function
The products are mains-operated medical suction devices designed for vacuum extraction, temporary surgical suction and bronchial suction in newborns. The product is employed during vacuum extraction to fix the baby’s head with the aid of an extraction cup. In addition, suction material (among other things: secretion, blood) is temporarily collected in a collection canister and subsequently disposed of. During operation, the pump generates vacuum in the secretion canister and hoses, by means of which the extraction cup can be fixed on the baby’s head. Furthermore, secretion, blood and body fluids can be suctioned. The fluid is collected in the secretion canister. The buttons allow you to set the final vacuum and thus the suction capacity in steps. The set value can be read on the vacuum display. Once the final vacuum is reached, the pump turns off and only continues working if suction capacity falls below the final vacuum value. Two vacuum extraction modes are available for vacuum extraction: • SEMI: The device automatically generates a base volume level of −20 kPa (−200 mbar; 150 mmHg). After reaching the base volume level, the user can check the correct positioning of the extraction cup. After confirming (by pressing button 1 (ON) for switching on automatic vacuum build-up), the device generates the desired final vacuum within the specified unit of time. Once the final vacuum has been reached, the device indicates this audibly and visually. • AUTO: The device automatically generates the desired final vacuum within the specified unit of time. Once the final vacuum has been reached, the device indicates this audibly and visually. After completing vacuum extraction or at any other time, the vacuum extraction mode can be stopped by pressing button 2 (OFF). The user can set the duration of the individual phases as well as the level of vacuum to be built up in the user menu.
1.5
Intended users
The device may only be used by trained and instructed medical professionals.
Introduction
9
1.6
Scope of delivery
Legend: Name
REF
Number
Basic device
1
Power cable 5 m
008.0629.0
2
Hydrophobic bacterial and viral filter
443.0738.0
3
Connecting hoses
999.0128.0
4
999.0127.0 Extraction hose, green, Ø 6 mm, L = 1.5 m
404.0146.0
5
Hose holder, for attachment to a standard rail
444.0450.0
6
Secretion canister 1.5 l (PC)
444.0100.0
7
Nipple set with overflow electrode
444.0012.0
8
Secretion canister lid incl. standard rail holder
444.0150.0
9
Trolley with standard rail ATMOS S 351
320.0070.0
10
Foot controller for ATMOS S 351
444.0478.0
11
Standard rail holder for Medi-Vac®
444.0451.0
12
Medi-Vac® outer canister 1 l
312.0473.0
13
Standard rail holder for Serres® complete
444.0484.0
14
Serres® outer canister
312.0465.0
15
Scope of delivery:
10 Introduction
Basic device name
REF
Includes number
ATMOS S 351 NATAL, 230 V
444.0401.0
1, 2
ATMOS S 351 NATAL, 100 V
444.0401.1
1, 2
ATMOS S 351 NATAL, 115 V
444.0401.2
1, 2
ATMOS S 351 NATAL, 127 V
444.0401.3
1, 2
ATMOS S 351 NATAL, 230 V
444.0491.0
1, 2, 3, 4, 6
ATMOS S 351 NATAL, 100 V
444.0491.1
1, 2, 3, 4, 6
ATMOS S 351 NATAL, 115 V
444.0491.2
1, 2, 3, 4, 6
ATMOS S 351 NATAL, 127 V
444.0491.3
1, 2, 3, 4, 6
ATMOS S 351 NATAL – basic set, 230 V
444.0490.0
1–9
ATMOS S 351 NATAL – basic set, 100 V
444.0490.1
1–9
ATMOS S 351 NATAL – basic set, 115 V
444.0490.2
1–9
ATMOS S 351 NATAL – basic set, 127 V
444.0490.3
1–9
ATMOS S 351 NATAL – basic set, 230 V (Medi-Vac®)
444.0492.0
1, 2, 3, 4, 5, 6, 12, 13
ATMOS S 351 NATAL – basic set, 230 V (Serres®)
444.0493.0
1, 2, 3, 4, 5, 6, 14, 15
ATMOS S 351 NATAL mobile, 230 V
444.0481.0
1–10
ATMOS S 351 NATAL mobile, 100 V
444.0481.1
1–10
ATMOS S 351 NATAL mobile, 115 V
444.0481.2
1–10
ATMOS S 351 NATAL mobile, 127 V
444.0481.3
1–10
ATMOS S 351 NATAL mobile with foot controller, 230 V 444.0482.0
1–11
ATMOS S 351 NATAL mobile with foot controller, 100 V 444.0482.1
1–11
ATMOS S 351 NATAL mobile with foot controller, 115 V 444.0482.2
1–11
ATMOS S 351 NATAL mobile with foot controller, 127 V 444.0482.3
1–11
1.7
Transport and storage
Only transport the product in a shipping carton that is padded and offers sufficient protection. If damage occurs during transport: 1. Document and report damages in transit. 2. Send the device to ATMOS; see chapter „6.3 Sending in the device“ on page 41. Ambient conditions for transport and storage: • Temperature:
−10...+60 °C
• Relative humidity:
30...95% without condensation
• Atmospheric pressure:
700...1060 hPa
Introduction 11
2
Notes for your safety
The safety of the ATMOS S 351 NATAL complies with the accepted standards of technology and the guidelines of the German Medical Devices Act.
2.1
General safety instructions
Familiarise yourself with the device in good time so that you are capable of operating it at any time. Only a fully functional product meets the safety requirements of users, patients and third parties. Therefore, please observe the following instructions on your product: Never operate the device if it shows any obvious safety defects.
2.2
Danger for users, patients and third parties
Electric shock due to unsuitable mains power connection, incorrect handling of the product or damage to product components. Burns, cardiac arrhythmias and even fatal injury are possible. •
Do not operate the device if it has been dropped. In this case, clean and disinfect the device and send it to ATMOS for repair.
•
Prior to each use, check for damage to the device and the power cable. Do not operate the device if you notice any damage. In this case, clean and disinfect the device and send it to ATMOS for repair.
•
You can only disconnect the device from the mains power supply by pulling out the power plug.
•
Position the device in such a way that you can easily disconnect it from the mains power supply at any time.
•
When disconnecting the device from the mains power supply, pull the power plug first and then the device plug.
•
Disconnect the device from the mains power supply before cleaning or disinfecting it.
•
Never touch the power plug or power cable with wet hands.
•
Never immerse the device in water or other liquids.
•
The device is not sterilisable.
•
Use the power cable only in dry surroundings. The surroundings must be non-conductive.
•
Ensure that no liquid enters the device. If liquid gets into the device, operation of the device must cease immediately. In this case, clean and disinfect the device and send it to ATMOS for repair.
•
Only use original accessories and original spare parts from ATMOS. This applies to the power cable in particular.
•
Follow the instructions on periodic tests in chapter „6 Maintenance and service“ on page 38.
•
Assembly, new settings, alterations, extensions and repairs may only be carried out by authorised persons.
•
Do not modify the device without the manufacturer’s permission.
12 Notes for your safety
Risk of infection due to patient secretion on the device! Deadly diseases can be transmitted. •
Always wear disposable gloves if you could come into contact with secretion.
•
Never use components marked with 2 more than once. These components are intended for single use only.
•
Sterile-packed parts may only be used if the packaging is undamaged.
•
Do not operate the device without a bacterial filter.
•
Before each use, check that the bacterial filter is dry and clean to ensure that it operates correctly.
•
A suction catheter, suction attachment or suction instrument must always be connected to the suction hose. The suction hose must never come into direct contact with the suction area.
•
Clean and disinfect the device after every use.
•
Clean and disinfect the device according to the operating instructions.
•
The device must not be used following oversuction.
Ensure that the device is always functional and ready for use. Your patient can be severely injured. •
Ensure that the device is always ready for use.
•
Place the device where it is easily accessible.
•
Perform a function check after each use.
•
ATMOS recommends always having another suction device ready at hand. That way you can also perform suctioning if a device should fail.
•
Please observe the notes on the electromagnetic compatibility (EMC) of the device.
Avoid improper use (vacuum extraction). The baby can be severely injured. •
You as the treating user are responsible for the proper procedure and techniques! The appropriateness and the kind of application must be decided by a trained doctor on a case-by-case basis.
•
The level of preselected vacuum and the selection of additional products must be made for all applications according to the corresponding specialist.
•
Vacuum values that are too high can lead to tissue damage.
•
Vacuum values that are too low can cause the extraction cup to tear off.
•
Always use a secretion canister having a minimum capacity of 1 litre.
•
Check the vacuum continuously during vacuum extraction.
•
Only use transparent hoses or hoses intended for vacuum extraction.
•
During vacuum extraction, the vacuum must be built up slowly in a controlled manner.
•
During vacuum extraction, the system must not be ventilated suddenly while simultaneously pulling on the extraction cup.
•
Using the foot controller during vacuum extraction disables the vacuum extraction automatic mode.
•
Vacuum extraction is not possible at elevated altitudes, as it may not be possible to achieve the vacuum required.
Notes for your safety 13
Avoid improper use (suction). Your patient can be severely injured. •
Employ the device only according to its intended use.
•
The product may only be used by medically trained persons who have been instructed in the handling of the medical suction system.
•
Please select the vacuum according to the patient and the application.
•
Observe the valid guidelines.
•
Observe the notes on hygiene and cleaning.
Explosion and fire hazard. There is a risk of burns and injuries. •
Never suction any explosive, flammable or corrosive gases or liquids. Please observe the intended use in chapter „1.3 Intended use“ on page 7.
•
Never operate the product in potentially explosive areas or in areas that are oxygenated.
•
Only use original accessories and original spare parts from ATMOS. This applies to the power cable in particular.
Tripping hazard due to cables. Injuries and fractures are possible. •
Lay the power cable properly.
WARNING Contact may cause allergic reactions! The materials used have been tested for their tolerability. In very rare cases, contact with accessible materials on the device and its accessories may cause allergic reactions. This applies in particular to contact injuries in conjunction with prolonged contact. If this occurs, seek medical attention immediately. Only a fully functional product meets the safety requirements of users, patients and third parties. Therefore, please observe the following instructions on your product:
2.3
Avoiding damage to the device
Storage and operation in an unsuitable environment. The electronics can become damaged. •
Please observe the ambient conditions for transport, storage and operation.
•
Always place the device on firm, level ground. The device must always be in a vertical position when you use it. Otherwise, secretion may enter the device.
14 Notes for your safety
ATTENTION Damage to device due to heat build-up! The device may become damaged. •
Do not cover the device during suction.
•
Keep the device and the power cable away from other heat sources.
•
Do not place the device directly next to other devices as this may cause excessive heating of the device. ATTENTION
Damage to the device due to improper use! The device may become damaged. •
Ensure that no liquid enters the device. Once liquid has entered the device, it may no longer be used. In this case, clean the device and send it to ATMOS for repair.
•
Always place the device on firm, level ground. The device must always be in a vertical position when you use it.
•
Use only power cables and extension cords that function properly.
Notes for your safety 15
3
Setting up and starting up
3.1
Device overview
Front view 1 2
5
3
4 6
1
3 2
7
4 5 6 7
ON / OFF switch Display Support for canister system Bacterial filter Connection for suction hose Secretion canister lid Connection for extraction cup
Rear view 1 2 1
3 4
2 3 4
5
16 Setting up and starting up
5
Pump connection Connection for foot controller Service interface for data read-out Potential equalisation Mains supply
3.1.1 Secretion canister Reusable canister system 1
7
2
6
3
5
1
Locking handle
2
Knurled screw for locking the lid insert and for adjusting the clamping force
3
Release button
4
Fill-level sensor with anti-foaming device
5
Lid rim
6
Aperture for double hose connector
7
Contacts for fill-level monitoring
1
Angle (connection for disposable suction hose)
2
Serres® suction liner
3
Serres® outer canister
4
Grey angle on the Serres® outer canister (connection for vacuum hose)
1
Angle (connection for disposable suction hose)
2
Red hose
3
Medi-Vac® suction liner
4
Connection for vacuum hose
5
Medi-Vac® outer canister
4
Disposable canister system Serres® canister system
4
3
2
1
Medi-Vac® canister system 2
1 4
3 5
Setting up and starting up 17
Device suspension for Serres®
3.2
Support for Medi-Vac®
Preparing the device
Read the safety information in chapter „2 Notes for your safety“ on page 12 carefully before using the product. Damaged pump diaphragms due to cold temperatures during transport. 1. In case the device was transported at temperatures below −5 °C: let the device stand at room temperature for at least 6 hours before proceeding with the next steps 2. Check the device, secretion canisters, power cable, accessories and hoses for possible damage. 3. If the device is damaged: document and report the damages in transit. Send the device to ATMOS (chapter „6.3 Sending in the device“ on page 41). 4. If the device is not damaged: place the device on a safe, level surface.
3.3
Connecting to the mains power supply
1. Check whether the voltage and frequency data listed on the device correspond to the values of the mains power supply. 2. Connect the device to the mains. 3. Secure the power cable against accidental removal by using the safety clamp.
18 Setting up and starting up
3.4
Connecting the secretion canister system and hoses 1. The anti-foaming device must be placed on the fill-level sensor for strongly foaming secretion. 2. Slide the secretion canister lid with the release button pointing forward onto the secretion canister. & Make sure that the lid rim is under the bead of the secretion canister. This seals the secretion canister tightly and the desired vacuum can be built up in the secretion canister. 3. Press the locking handle downwards until it clicks into place. 4. Hang the secretion canister in the left or right support for the canister system. Using the support for the canister system for purposes other than what it was designed for can cause malfunctions. 1. Push the double hose connector into the canister lid twisting gently. »
The double hose connector locks into place.
1. Connect a short hose to the pipe connection on the device and to the bacterial filter. 2. Connect a longer hose to the printed side of the bacterial filter and to the vertical fitting of the double hose connector. Never operate the device without a bacterial filter. 1
2
3
1. Connect the suction hose (Ø 10 mm) to the angled fitting (2) of the double hose connector. & Use a hose reducer (3) for suction hoses with a Ø of 6 mm. 2. Use the vacuum extraction suction hose to join the horizontal fitting (1) of the double hose connector with the extraction cup.
Setting up and starting up 19
4
Operation
4.1
Ambient conditions during operation
• Temperature:
+5 ... +40 °C
• Relative humidity:
30 ... 95% without condensation
• Atmospheric pressure:
700 ... 1060 hPa
4.2
Control panel S 351 NATAL
3
ON
OFF
1
2
4
high vacuum / high flow
- + 5
6
1
Button for switching on the automatic vacuum build-up (ON)
2
Button for switching off the automatic vacuum build-up (OFF)
3
LEDs for indicating the active function
4
Display
5
Button for reducing the vacuum
6
Button for increasing the vacuum
7
Button for selecting the maximum vacuum
4.3
MAX 7
Switching on the device
1. Press the ON / OFF switch.
20 Operation
»
The start screen appears.
»
The pump starts. The pump starts automatically in the stored vacuum extraction mode (SEMI or AUTO).
»
By pressing button 2 (OFF), you stop vacuum extraction mode and are immediately redirected to suction mode.
»
The ON / OFF switch remains lit as long as the device is on.