Atmos Record 55 DDS User manual

Operating Instructions
ATMOS Record 55
DDS
English
GA1GB.210202.0
2020_06 Index 26
0124

2
Table of contents
1 Introduction.......................................................................................................4
1.1 Notes on operating instructions ..............................................................................4
1.2 Explanation of pictures and symbols ......................................................................5
1.3 Intended use...............................................................................................................7
1.4 Function.......................................................................................................................7
1.5 Intended users ...........................................................................................................8
1.6 Scope of delivery........................................................................................................8
1.7 Transport and storage...............................................................................................9
2 Notes for your safety......................................................................................10
2.1 General safety instructions.................................................................................... 10
2.2 Danger for users, patients, and third parties ...................................................... 10
2.3 Avoiding damage to the device ............................................................................. 12
3 Setting up and starting up .............................................................................13
3.1 Device overview....................................................................................................... 13
4 Operation.........................................................................................................14
4.1 Initial start-up .......................................................................................................... 14
4.2 Preparing the device............................................................................................... 14
4.3 Assembly of the DDS secretion canister .............................................................. 14
4.4 Using the DDS splash protection .......................................................................... 14
4.5 Attaching/removing the DDS canister lid ............................................................. 14
4.6 Inserting/removingtheDDSbacteriallter/oversuctionstop......................... 15
4.7 Attaching, closing, and opening the DDS secretion canister handle................ 15
4.8 Attaching/removing the DDS secretion canister ................................................. 15
4.9 DDS secretion canister hose holder ..................................................................... 15
4.10 Inserting the DDS hose adapter............................................................................ 16
4.11 Connecting the suction hose ................................................................................. 16
4.12 Suctioning ................................................................................................................ 16
4.13 DDS changeover docking station .......................................................................... 17
4.14 Options..................................................................................................................... 17
5 Reprocessing....................................................................................................18
5.1 Safety instructions for reprocessing..................................................................... 18
5.1.1 General safety instructions............................................................................... 18
5.1.2 Danger for users, patients, and third parties................................................. 18
5.1.3 Avoiding damage to the device........................................................................ 18
5.2 Preparing/completing reprocessing ..................................................................... 19
5.3 Preparing surfaces .................................................................................................. 19
5.3.1 Overview ............................................................................................................. 19
5.3.2 Selecting process chemicals............................................................................. 19
5.3.3 Pre-cleaning........................................................................................................ 20
5.3.4 Wipe disinfection ............................................................................................... 20
5.4 Reprocessing the accessories................................................................................ 20
5.4.1 Overview ............................................................................................................. 20
5.4.2 Secretion canister system................................................................................. 21
5.4.3 Hoses................................................................................................................... 23
6 Maintenance and service...............................................................................24
6.1 Periodic tests ........................................................................................................... 24

3
6.2 Function check......................................................................................................... 24
6.3 Sending in the device.............................................................................................. 24
6.4 Reprocessing by the manufacturer....................................................................... 24
7 Troubleshooting ..............................................................................................25
7.1 Troubleshooting ...................................................................................................... 25
8 Accessories ......................................................................................................26
9 Consumables ...................................................................................................27
10 Disposal............................................................................................................28
11 Technical data .................................................................................................29
12 Notes on EMC ..................................................................................................30
13 Notes ................................................................................................................31
Further information, accessories, consumables,
and spare parts are available from:
ATMOS
MedizinTechnik GmbH & Co. KG
Ludwig-Kegel-Straße 16
79853 Lenzkirch
Germany
Phone [phone]
FAX [phone] (Switchboard)
FAX [phone] (Service)
E-mail: [email protected]
Web: www.atmosmed.de

4Introduction
1 Introduction
1.1 Notes on operating instructions
These operating instructions contain important instructions on how to
operateyourproductsafely,correctly,andeectively.
These operating instructions are designed for training and instructing
new operating personnel in the use of the system, and also 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 device.
Care, periodic tests, regular cleaning, and proper use 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 are
familiar with the product. The person in question must possess the test
devices and original spare parts required to carry out these measures.
Read chapter ‘Notes for your safety’ on page 10 before using the
productforthersttime.Thiswillhelpyoutoavoidpotentiallydanger-
ous situations.
The product bears CE marking CE 0124 according to the EC directive
93/42/EEC of the council for medical products and meets the basic
requirements of appendix I of this directive.
The product complies with all applicable requirements of Directive
2011/65/EU on the restriction of the use of certain hazardous sub-
stances in electrical and electronic equipment (“RoHS”).
The Declaration of Conformity and our general standard terms and
conditions can be viewed on our website at www.atmosmed.com.
ThequalitymanagementsystematATMOShasbeencertiedaccord-
ing to international standard EN ISO 13485.
These operating instructions are valid for the following products:
ATMOS Record 55 DDS REF 444.0910.0
ATMOS Record 55 DDS 100 V REF 444.0910.1
ATMOS Record 55 DDS 115 V REF 444.0910.2
ATMOS Record 55 DDS 127 V REF 444.0910.3
ATMOS Record 55 DDS (2 x 3 l secretion
canister)
REF 444.0930.0
ATMOS Record 55 DDS (2 x 5 l secretion
canister)
REF 444.0940.0

5Introduction
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 neces-
sary measures.
Warning of a danger that can cause fatal or serious injury.
Useful information on the handling of the device.
1. Action. Proceed step by step.
»Result of an action.
Move in this direction, plug in.
On device and type plate
Follow operating instructions (blue)
Observe the operating instructions
Warning; take extra care to observe
0124
This product complies with the relevant requirements of the EU Directives.
This product complies with the relevant requirements of the EU Directives.
Foot switch
Manufacturer
Manufacturing date

6Introduction
GOSTCerticate(Russia)
Eurasian conformity
SN Serial number
REF Order number
EAN European Article Number
IPX1 Protection against the ingress of damaging moisture (dripping water)
Applied part type BF
Professional disposal
For single use only (symbol located on consumables)
NON
STERILE
Not sterile
AUTOCLAVE
Autoclavable
PATIENT Connection for suction hose/patient
Potential equalisation
Protection class II
Fuse
Alternating current
On, connected to the power supply
AP Class AP (for use in potentially explosive areas)

7Introduction
1.3 Intended use
Main function: Suctionofsecretions,blood,serousuids,rinsinguids,and
forthetemporarycollectionoftheseuids.
Medical indications/
application:
For all applications where suction is needed, such as in
general surgical procedures (e.g., suction of wound cavities,
abscesses), the nasopharyngeal cavity, for endoscopy, for
suctionofsecretionorrinsinguids,andinneurosurgery.
For subcutaneous liposuction.
Specication of the
main function:
Forthedrainageandtemporarycollectionofbodyuids.By
means of an electric suction pump, a negative pressure is
created. An additional secretion canister must be attached to
allowthetemporarycollectionofdrainedbodyuids.
User prole: Doctors,medicalsupportstawithoutrestrictions.
Patient groups: Patients of all ages with and without restrictions.
Application organ: Naturaloricesaswellasopeningsthatresultfromasurgical
intervention (entire body of humans and animals).
Application time: For short-term use on patients (< 30 days)
Area of application: The application site is the clinical, outpatient, and veterinary
eld.Thedevicemayonlybeusedbypersonswhohave
received the relevant training and instruction.
Contraindications: Not suitable for:
• Drainage operations in the low-vacuum range (e.g.,
thoracic or wound drainage)
• Use outside the medical sector
• Suctionofammable,corrosive,orexplosivesubstances
• Suction in potentially explosive atmospheres
• Not suitable for use as a vacuum extraction system
The product is: Active
Sterility: No sterile product
Single-use product/
re-sterilisation:
The device and parts of the accessories are reusable. Informa-
tion on reprocessing, cleaning, and disinfection can be found
in this document.
1.4 Function
The ATMOS Record 55 DDS is a mains-operated surgical suction device, the core of
which is a high-performance, maintenance-free diaphragm pump. It generates vacuum
inthehoseandrinsingcanistersystemwhichassistsindrawingoandcollectingthe

8Introduction
secretions.Viaavacuumregulatorwithvacuumgauge,thenalvacuumandthusthe
desired suction capacity can be precisely adjusted.
Severalsecretioncanistersofdierentsizesareavailableforsecretioncollection.The
reusable secretion canister can be mounted to the ATMOS Record 55 via the Direct
Docking System. The user can connect the suction hose directly. A hydrophobic bacterial
lterlocatedinthelidofthecanisterpreventsbacteriaandliquidsfromenteringthe
pump.Thislterprotectsthedeviceagainstoversuction.Theintakelocatedinthehose
connection prevents foaming in the secretion canister and therefore ensures a longer
lterlife.
1.5 Intended users
May only be used by trained professionals in supervised and medical operations.
1.6 Scope of delivery
Basic device ATMOS Record 55 DDS
ATMOS Record 55 DDS (230 V, 100 V, 115 V, 127 V) REF
1x power cable 5 m 008.0629.0
1x hose holder 443.0003.0
ATMOS Record 55 DDS (2 x 3 l secretion canister) REF
1x power cable 5 m 008.0629.0
1x hose holder 443.0003.0
2x DDS secretion canister, plastic 3 l, autoclavable 340.0051.0
2x DDS canister lid with sealings, autoclavable 340.0053.0
2x DDS canister handle, grey, autoclavable 340.0055.0
2x DDS splash protection, silicone, autoclavable 340.0056.0
1x DDS hose adapter set (Ø 6 mm + Ø 10 mm), autoclavable 340.0057.0
12xDDSbacteriallter 340.0054.0
1x suction hose (silicone), Ø 6 mm, L = 2 m 000.0361.0
ATMOS Record 55 DDS (2 x 5 l secretion canister) REF
1x power cable 5 m 008.0629.0
1x hose holder 443.0003.0
2x DDS secretion canister, plastic 5 l, autoclavable 340.0052.0
2x DDS canister lid with sealings, autoclavable 340.0053.0

9Introduction
2x DDS canister handle, grey, autoclavable 340.0055.0
2x DDS splash protection, silicone, autoclavable 340.0056.0
1x DDS hose adapter set (Ø 6 mm + Ø 10 mm), autoclavable 340.0057.0
12xDDSbacteriallter 340.0054.0
1x suction hose (silicone), Ø 6 mm, L = 2 m 000.0361.0
1.7 Transport and storage
Onlytransportthedeviceinashippingcartonthatispaddedandoerssucient
protection.
If damage occurs during transport:
1. Document and report damages in transit.
2. Send the device to ATMOS; see chapter 24‘6.3 Sending in the device’ on page 24.
Ambient conditions for transport and storage:
• Temperature: −30...+50°C
• Relative humidity: 5...90% without condensation
• Air pressure: 700...1060hPa

10 Notes for your safety
2 Notes for your safety
2.1 General safety instructions
Only a fully functional product meets the safety requirements of users, patients, and
third parties. Therefore, observe the following instructions on your product:
Please read and pay attention to the safety instructions prior to using the product.
2.2 Danger for users, patients, and third parties
WARNING
Choking hazard for children due to accessories!
Children can strangle themselves or choke on small parts.
• Keep children away from hoses and connection cables.
• Keep children away from swallowable small parts. Examples of such swallowable
smallpartsarethengertipandsealingring.
CAUTION
Explosion and re hazard!
Burns and injuries are possible.
• Neversuctionanyexplosive,ammable,orcorrosivegasesorliquids.Pleaseob-
serve the intended use in chapter ‘1.3 Intended use’.
• Never operate the product in potentially explosive areas or areas that are oxygenat-
ed.
• Only use original accessories and original spare parts from ATMOS.
WARNING
Your patient can be severely injured.
Avoid misuse.
• The product may only be used by medically trained persons who have been instruct-
ed in the handling of the medical suction system.
• Theproductmayonlybeusedbyqualiedpersonnelinsupervisedoperation.
• Select the vacuum according to the patient and the application.
• Observe the valid guidelines.
• Always set up the unit in such a way that the operating elements are in clear view
and within easy reach of the operator. The device must be set up on a stable, level
surface.

11Notes for your safety
WARNING
Ensure that the device is always functional and ready for use.
Yourpatientcouldsuocate.
• Before connecting the device, check whether the required mains voltage on the
device matches the mains voltage of the mains power supply.
• Position the device in an easily accessible location and keep access free.
• Make sure that the power cable is working. Replace defective accessories immedi-
ately.
• Removethetransportprotectiononthebottomofthedevicepriortorstuse.
• ATMOS recommends always having another suction device ready at hand. That way
you can also perform suctioning if a device should fail.
WARNING
Risk of infection due to pathogens on the product!
Deadly diseases may be transmitted.
• Always wear disposable gloves if you might come into contact with secretion.
• Always wear disposable gloves when using the product.
• Never use components that are marked with 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lter.
• A suction catheter, hose-rinsing aperture, or medical suction set must always be
connected to the hose. The suction hose must never come into direct contact with
the suction area.
• Clean and disinfect the product after every use.
• Clean and disinfect the product according to the operating instructions.
• The product must not be used following oversuction.
WARNING
Tripping hazard due to cables.
Injuries are possible.
• Lay connecting cables properly.

12 Notes for your safety
WARNING
Electric shock due to unsuitable mains connection, incorrect handling of the
product, or damaged product components
Burns, cardiac arrhythmias, and even fatal injury are possible.
• Prior to each use, check for damage to the device and the power cable. Do not oper-
ate the device if you notice any damage. In this case, clean and disinfect the device
and send it to ATMOS for repair.
• Disconnect the device from the mains power supply prior to cleaning or disinfection.
• You an only disconnect the device by removing the power plug from the mains
power supply.
• Position the device in such a way that you can easily disconnect it from the mains
power supply at any time.
• Only connect the device to a mains power supply with a protective conductor.
• Never touch the plug or power cable with wet hands.
• Only use the power cable in dry surroundings. The surroundings must be non-con-
ductive.
• Ensure that no liquid penetrates the device. If liquid has entered the device, op-
eration of the device must cease immediately. In this case, clean and disinfect the
device and send it to ATMOS for repair.
• Only use proper power cables and extension cords.
• Never touch the device's interfaces and the patient at the same time!
• Only use original accessories and original spare parts from ATMOS.
• Pay attention to the periodic tests in chapter ‘6 Maintenance and service’.
• 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.
2.3 Avoiding damage to the device
ATTENTION
Storage and operation in an unsuitable environment.
The product may become damaged.
• Please observe the ambient conditions regarding transport, storage, and operation.
• After transporting the device at low temperatures, keep it at room temperature for
at least six hours before initial start-up. If the device is not acclimatised, it may not
be used, as the diaphragm of the pump could become damaged.

13Setting up and starting up
3 Setting up and starting up
3.1 Device overview
Front view
Vacuum gauge
Vacuum regulator
On/oswitch
DDS canister handle
DDS canister lid
DDS secretion canister
Connection for the foot controller or
foot switch (optional)
Rear view



Connection for potential equalisa-
tion
Equipment safety fuse
Mains supply
Vacuum connection: Direct Docking System
The vacuum connection between
the pump and secretion canister
system is immediately established
when the DDS canister is attached!
Risk of injury and risk of infection due to production residues.
1. Priortorstuse,preparetheproductaccordingtotheoperatinginstructions.

14 Operation
4 Operation
4.1 Initial start-up
Observe the safety instructions prior to initial start-up!
Remove the transport protection on the bottom of the device by loosening the two
Allen screws marked in red.
The transport protection screws must be inserted again before returning the device.
After transporting the device at low temperatures, it should be kept at room temper-
ature for at least six hours before initial start-up; otherwise, the device may not be
operated.
4.2 Preparing the device
• Check whether the voltage and frequency data listed on the device correspond to
the values of the mains power supply and then connect it to the mains.
For surgical procedures, we recommend additionally connecting the device via the
connection to the potential equalisation of the examination room.
» The device is now ready for use.
4.3 Assembly of the DDS secretion canister






DDS secretion canister handle
DDSbacteriallter
DDS hose adapter
DDS canister lid
DDS splash protection
DDS secretion canister
4.4 Using the DDS splash protection
1. Attach the splash protection to the pipe connec-
tion in the DDS canister lid.
The splash protection protects the DDS bacterial
lterfrombecomingwettedprematurelyby
liquids and/or foam formation.
4.5 Attaching/removing the DDS canister lid
1. PlacetheDDSsecretioncanisteronarmsurfaceandset the DDS secretion canis-
ter lid horizontally on it (the lid cannot be turned incorrectly).
2. Gently press the DDS canister lid with both hands onto the secretion canister.

15Operation
3. To open the DDS canister lid, hold it on the reinforcement bars of the mounting
xtureandthenpulltheDDScanisterlidupandobyreachingintotheopeningfor
thelter.
4.6 Inserting/removing the DDS bacterial lter /
oversuction stop
TheDDSbacteriallter/oversuctionstoparedispos-
able products.
Before each use, check whether the DDS bac-
teriallter/oversuctionstopisdryandclean.
ReplacetheDDSbacteriallterwithanewDDS
bacteriallterifitisdiscolouredorcontaminated
or if oversuction has occurred.
1. InsertthebacteriallterintotheDDSsecretion
canister handle.
4.7 Attaching, closing, and opening the DDS secretion
canister handle
1. To attach the DDS secretion canister handle,
insert it into the grooves of the canister lid (with
the locking latches open).
2. To close the DDS secretion canister handle, clip
the locking latches under the canister rim. Then
press the clips towards the secretion canister
until they click into place.
3. To open, pull the clips outwards and remove the
locking latches from under the canister rim.
4.8 Attaching/removing the DDS secretion canister
1. To attach the DDS secretion canister, allow it to
slide vertically downwards into the mounting
xture.
2. To remove the DDS secretion canister, lift it
straight up.
4.9 DDS secretion canister hose holder
1. If using a DDS secretion canister hose holder,
attach it between the canister lid and the hose
adapter.

16 Operation
4.10 Inserting the DDS hose adapter
1. Insert the DDS hose adapter (Ø 6 or 10 mm) into
the ‘Patient’ opening on the DDS canister lid.
2. Turn it slightly and press it down.
The adapter can be removed again by turning it
slightly.
4.11 Connecting the suction hose
Connect the suction hose to the already inserted
hose adapter.
4.12 Suctioning
1. Please ensure that the following parts have been
reprocessed prior to treating a new patient:
• Suction hose including hose-rinsing aperture or
suction instruments
• DDS secretion canister system including DDS
canister lid and DDS hose adapter
2. Prior to each use, check whether the DDS bac-
teriallterwasinsertedduringcleaningand
disinfection.
3. Replacethebacteriallterwithanewbacterial
lterifitisdiscolouredorcontaminated,orif
oversuction has occurred.
4. Switch on the device.
5. Close the suction hose and set the desired
vacuum.
6. Connect the suction catheter, hose-rinsing
aperture, or suction instruments.
Observe the liquid level in the secretion canister during suction. The DDS bacterial
lterpreventsliquidfrombeingsuckedintothepump.Nevertheless,thesecretion
canister should be emptied or replaced when it is 2/3 full (including foam crown).
Ifliquidhasbeensuckedintothepumpdespitethebacteriallter,thedevicemay
not be operated again until it has been checked by an authorised service partner.

17Operation
4.13 DDS changeover docking station
The maximum load of the station is 15 kg; higher
loads may damage the device!
The DDS changeover docking station is used if two
secretion canisters are required. The changeover
lever serves to switch the vacuum to the secretion
canister being used. When removing or attaching
a secretion canister, switch the lever towards the
second secretion canister.
4.14 Options
Foot switch REF 443.0755.0
Pneumaticallyexplosion-proofswitchforswitchingthedeviceonando.
1. Connect the foot switch.
2. Set the main switch in the control panel to foot
switch operation (OFF).
3. Pressing the foot switch turns the device on.
4. Pressing the foot switch again turns the device
o.
5. If the main switch in the control panel is set
to continuous operation (ON), the foot switch
produces noeect.
Foot controller REF 443.0770.0
For regulating the vacuum.
Connect the foot controller (remove the protection
cap and tighten the nut on the foot controller hose).
1. To increase the vacuum, press the pedal down.
2. Whenyouliftoyourfoot,thecontrollerlocksin
that position.

18 Reprocessing
5 Reprocessing
5.1 Safety instructions for reprocessing
5.1.1 General safety instructions
We recommend that you always document all maintenance work and part replacements
in writing.
It is the responsibility of the user to ensure that the demands for cleaning and disinfec-
tion are adhered to. Generally, validation and routine monitoring of the procedure will
be necessary.
Reprocessing may only be carried out by persons who have the necessary expertise. The
person in question must have the necessary equipment to carry out these measures.
5.1.2 Danger for users, patients, and third parties
Risk of infection due to unsuitable accessories.
Deadly diseases may be transmitted.
• Always wear your own personal protective gear. The protective gear consists of
protective gloves, protective clothing, goggles, and mouth and nose protection for all
steps in which the product components are still contaminated.
• Only use aids that can be easily reprocessed or ones that are disposable products.
Risk of infection due to unsuitable reprocessing.
Deadly diseases may be transmitted.
• Make sure that all areas of the accessories can be easily reached.
• Only use suitable load carriers for mechanical reprocessing. This especially applies
to accessories with hollow spaces and lumens that are hard to reach.
• Make sure that air bubbles do not form in the hollow spaces and lumens of accesso-
ries when placing them in processing solutions.
5.1.3 Avoiding damage to the device
Damage to the device due to cleaning with xatives.
Stains cannot be removed permanently.
• Do not use aldehydes before and during cleaning.
• Donotexposetheproducttotemperatures>40°C/104°Fbeforeandduring
cleaning.
Unsuitable aids.
Follow the corresponding operating instructions of all aids and devices used.

19Reprocessing
Unsuitable cleaning agents and disinfectants.
The product may become damaged.
• Do not use any process chemicals containing the following ingredients on plastic
parts:
• Chloramides or phenol derivatives
• Do not use any process chemicals containing the following ingredients on stainless
steel:
• Organic or inorganic bases
• Alkaline solutions
Incorrect mechanical cleaning and disinfection.
Corrosion due to moisture.
• Removetheproductsimmediatelyaftertheprogrammeisnished.
5.2 Preparing/completing reprocessing
Prior to reprocessing
1. Disassemble the product for reprocessing into the following items:
• Device
• Hoses
• Secretion canister system
After reprocessing
1. Perform a function check.
5.3 Preparing surfaces
5.3.1 Overview
Surface After each application After each patient Daily Weekly Every 14 days Monthly Pre-cleaning Wipe cleaning Wipe disinfection Spray disinfection Remarks
Housing x x x
5.3.2 Selecting process chemicals
Alwaysobservethemanufacturer’sspecicationsfortheprocesschemicals.
Cleaning agent
(manufacturer) Active ingredients in 100 g Type Housing
Disinfection

20 Reprocessing
Cleaning agent
(manufacturer) Active ingredients in 100 g Type Housing
Green & Clean SK
(Metasys)
<1 g dialkyldimethylammonium chloride, <1 g alkyldimethylethylbenzylam-
monium chloride, <1 g alkyldimethylbenzylammonium chloride
Foam
Ready to use
x
Dismozon® plus
(Bode Chemie)
95.8 g magnesium monoperoxyphthalate hexahydrate Granulate x
Kohrsolin® FF (Bode
Chemie)
5 g glutaral, 3 g benzyl-C12-18-alkyldimethylammonium chloride, 3 g
didecyldimethylammonium chloride
Liquid
concentrate
x
Kohrsolin® extra
(Bode Chemie)
14.1 g (ethylenedioxy)dimethanol, 5 g glutaral, 8 g didecyldimethylammo-
nium chloride
Liquid
concentrate
x
Perform® (Schülke
& Mayr)
45 g pentapotassium bis(peroxymonosulphate) bis(sulphate) Powder x
Mikrobac® forte
(Bode Chemie)
19.9 g benzyl-C12-18-alkyldimethylammonium chloride, 5 g N-(3-amino-
propyl)-N-dodecylpropane-1,3-diamine
Liquid
concentrate
x
Bacillol® 30 Foam
(Bode Chemie)
14 g ethanol, 10 g propan-2-ol, 6 g propan-1-ol, 0.5 g n-alkyl-aminopro-
pyl-glycine
Foam, ready
to use
x
Incidin® Active
(Ecolab)
Peracetic acid Powder x
mikrozid® sensitive
wipes (Schülke &
Mayr)
0.26 g alkyl(C12-16)dimethylbenzylammonium chloride, 0.26 g dide-
cyldimethylammonium chloride, 0.26 g alkyl(C12-14)ethylbenzylammonium
chloride
Wipes x
5.3.3 Pre-cleaning
1. Disconnect the device from the mains power supply.
2. Clean the surface evenly with a suitable cloth and clear water. Pay particular atten-
tion to hard-to-reach areas.
» No more residue is visible.
5.3.4 Wipe disinfection
Alwaysobservethemanufacturer’sspecicationsfortheprocesschemicals.
5.4 Reprocessing the accessories
5.4.1 Overview
Accessories Disposable product Max. reprocessing cycles After each application After each patient Daily Weekly Every 14 days Monthly Pre-treat Pre-cleaning Manual cleaning and disinfection Mechanical cleaning and disinfection Sterilisation
Secretion canister system
• DDS secretion canister260 x x x x x
• DDS canister lid260 x x x x x
DDS secretion canister handle
DDS splash protection
DDS hose adapter