Nouvag DP 30 LipoPlus User manual

DispenserDP30LipoPlus
Instructions for use
EN

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved
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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
CONGRATULATIONS ON YOUR PURCHASE OF A PRODUCT FROM NOUVAG.
We are pleased that you have chosen a quality product from NOUVAG and thank you very much for the trust you
have placed in us.
These instructions for use will familiarize you with the device and its functions so that you can apply and use
them correctly.
SYMBOLS
General warning sign General
mandatory action
Refer to
instructions for use
Manufacturer Date of manufacture Use-by date
Do not use if the
package is damaged Not for reuse Separate collection required (WEEE)
Biological hazard Not made with natural
rubber latex
Contains or presence
of Phthalate
Batch code Catalog number Serial number
Medical device EOSTERILE Sterilized using
ethylene oxide
Authorized represen-
tative in the European
Community
Water resistance Equipotentiality Indication of pump
flow direction
Type BF applied part Foot switch
0197
European Conformity
mark
Certified by the TÜV
Rheinland North
America Group

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 3
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
CONTENT
INTENDED PURPOSE 4
Medical indications
Contraindications
Side effects
Intended users
Target population
Ambient conditions
SAFETY INFORMATION 5
Modifications and misuse
Essential requirements
During use
SCOPE OF DELIVERY 6
DEVICE OVERVIEW 7
Front view
Rear view
SETUP 8
Device and accessories setup
Connection to the power supply
Potential equalization connection according to DIN42801
Device preparation
OPERATION 10
Switching the device on and off
Regulation of the infiltration process
Peristaltic pump
Functional check
CLEANING AND DISINFECTION 10
Control unit and foot switch
Tubing set REF6022
MAINTENANCE 11
Replacing the control unit fuses
Safety inspections
MALFUNCTIONS AND TROUBLESHOOTING 12
ACCESSORIES AND SPARE PARTS 13
Information on disposal
TECHNICAL DATA 13
WARRANTY COVERAGE 14
Post market surveillance
Service points
APPENDIX 15

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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
INTENDED PURPOSE
MEDICAL INDICATIONS
The DispenserDP30LipoPlus is an infiltration pump, that is used in combination with a foot pedal and a sterile
single use tubing set (independent medical devices) to infiltrate tumescent solution (Klein solution) in the subcu-
taneous fat layer. The DispenserDP30LipoPlus is used in the following medical indication:
// Liposuction
CONTRAINDICATIONS
General contraindications concern patient health status, such as severe cardiopulmonary disease, local inflamma-
tion, sepsis, and coagulation disorders.
Specific contraindications include:
Infectious wounds Liposuction may only be performed after the treatment of the infection and necrotic tissue.
Liposuction shortly after a strict diet of the patient.
Morbid obesity (obesity) Large suction volumes increase the risk of death due to fluid shifts.
Intravascular infusion of liquids.
Infiltration of excessive volume of tumescent solution (mutiple liters).
Treatment of a excessive surface area.
SIDE EFFECTS
Side effects of infiltration of tumescent solution for liposuction are generally infrequent and minor.
Clinical literature reports the following side effects:
¬Inflammation (local/systemic)
¬Bleeding
¬Haematomas
¬Oedema
¬Fat/Pulmonary embolysm
INTENDED USERS
The device is designed to be used by professional and trained users only, in professional contexts (e.g. hospital,
clinic). The device is not to be used by patients or by untrained users.
TARGET POPULATION
Adults (>18 years old). See contraindications for limiting health factors.
AMBIENT CONDITIONS
TRANSPORT AND STORAGE DURING USE
Relative humidity max. 90 % max. 80 %
Temperature 0 °C – 60 °C 10 °C – 60 °C
Atmospheric pressure 700 – 1’060 hPa 800 – 1’060 hPa

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 5
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
SAFETY INFORMATION
Every use of the DispenserDP30LipoPlus different to the I  > causes risks for patients and
trained personnel. If physical examinations and therapies are carried out without use of the devices, then the
devices must be removed from the place of treatment. Avoid any connection or close adjacency to other devices.
MODIFICATIONS AND MISUSE
Modifications/manipulations on the DispenserDP30LipoPlus and its accessories are not permitted. Failure
to follow these instructions can have unpredictable consequences for the user, the patient or third parties.
For consequential complications, resulting from illicit modifications/manipulations the manufacturer
assumes no responsibility and the guarantee is void.
NOUVAG recommends the use of Klein tumescent anesthesia solution. The use of other solutions is on the
responsibility of the surgeon. When infiltrating tumescent anesthesia solution, do not exceed 0.05% w/w anes-
thetic concentration.
ESSENTIAL REQUIREMENTS
Do not use the device if the shipping box has holes/cracks on the flat surfaces, and/or if the Styrofoam protec-
tive packaging is broken.
The DispenserDP30LipoPlus may only be operated by qualified and trained personnel!
The use of third-party products is the responsibility of the operator. Functionality and patient safety cannot
be guaranteed with third-party accessories.
Repairs may only be performed by authorized NOUVAG service technicians!
Improper use or repair of the device, or failure to observe these instructions, relieves NOUVAG from any obli-
gation arising from warranty provisions or other claims.
Prior to using the device, before startup, and before operation, the user must always ensure that the device
and accessories are in good working order and are clean, sterile and operational.
Ensure that the operating voltage setting corresponds to the local mains voltage.
The DispenserDP30LipoPlus may only be operated under constant supervision of medical personnel. The
absence of a warning buzz to indicate malfunctions of the device requires the permanent control of the
volumetric displacement of the pump.
DURING USE
The device is not sterile on delivery. Please observe the instructions C   > .
Do not use device in the vicinity of flammable mixtures!
The use of the DispenserDP30LipoPlus other than that for which it was designed (see  M -
 > ) is not permitted. The responsibility is solely carried by the operator.

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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
SCOPE OF DELIVERY
REF DESCRIPTION QUANTITY
4181 Dispenser DP 30 LipoPlus control unit 1
6022 Disposable tubing set, sterile, 4 m 1
1770 Stand for irrigation fluid bottle 1
31628 Dispenser DP 30 LipoPlus instructions for use 1
SELECTIVELY: SET NO. 4161 – DISPENSERDP30LIPOPLUS CONTROL UNIT WITH ON/OFF FOOT SWITCH
REF DESCRIPTION QUANTITY
1527nou ON/OFF foot switch 1
SELECTIVELY: SET NO. 4163 – DISPENSERDP30LIPOPLUS CONTROL UNIT WITH VARIO FOOT SWITCH
REF DESCRIPTION QUANTITY
1511nou VARIO foot switch 1

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INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
DEVICE OVERVIEW
1Operating panel with pump displacement scale 2Pedal 3Control dial to set pump displacement volume 4Indicator light for
Power ON/OFF 5Release key for tubing set bracket 6Peristaltic pump 7Tubing set 8Stand for irrigation fluid bottle 9Roller
clamp 10Venting valve 11Irrigation fluid container 12Type plate with type designation, reference number, serial number, informa-
tion on power supply and device fuse 13Pedal socket 14Potential equalization 15Power plug socket 16Main switch 17Fuse
compartment
FRONT VIEW
REAR VIEW

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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
SETUP
DEVICE AND ACCESSORIES SETUP
¬Place the DispenserDP30LipoPlus and all required accessories and instruments on an even, non-slip surface
and make sure you have good access to all controls.
¬Do not allow the operating range of the device and accessories to be compromised by limiting factors.
¬The system display must be always fully visible.
¬It must be explicitly ensured that no objects can fall on the pedal.
¬The power plug at the rear of the device must be always accessible.
CONNECTION TO THE POWER SUPPLY
To prevent of risks of an electric shock, the device may only be connected to a power network with a PE
protective ground conductor!
If the voltage shown does not correspond to the local mains voltage, the grey fuse holder must be set to the cor-
rect voltage:
1 Unplug the power cable.
2 Use a screwdriver to open the fuse slot.
3 Remove the fuse holder.
4 Remove the grey fuse holder and reinsert it so that the local mains voltage setting is shown in the small
window.
5 Slide fuse holder back in and close the fuse slot.
6 Check the mains voltage shown on the fuse slot.
7 Plug the power cable back into the device.
POTENTIAL EQUALIZATION CONNECTION ACCORDING TO DIN42801
At the back of the device a potential equalization plug is installed, according to DIN42801.
The additional potential equalization has the task of equalizing potentials between different parts of conductive
materials that can be touched at the same time, or reducing potential differences.
This connection must be used, to protect the patient, the user and third parties from touch voltages.
The equipotential plug is marked with the following symbol:

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 9
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
DEVICE PREPARATION
1 Insert the stand for the irrigation fluid into the stand holder.
2 Plug the foot switch plug into the foot switch socket at the rear of the control unit.
3 Assemble the tubing set (see images).
Check the expiry date of the tubing set and ensure that the packaging is not damaged. Using non-sterile
tubing sets can result in serious infection and, in extreme cases, can cause death.
When inserting the tubing set, notice the arrow on the cover of the pump compartment. It indicates the flow
direction of the cooling liquid.
Use only NOUVAG tube sets, otherwise the correct function cannot be guaranteed.
Do not regulate the amount of irrigation fluid using the roller clamp on the tube set; with the
DispenserDP30LipoPlus, this is regulated instead using the control dial and the foot pedal. For this reason,
make sure to open the roller clamp as far as it will go.
The container of infiltration fluid may weigh a maximum of 2kg. Heavier containers can cause the device to
tip over
A Press the release key for tubing set bracket to open the pump.
B The compartment with the integrated tubing bracket opens.
C Place the tubing set into the tubing bracket provided in such a way that the end of the tubing set with
the spike exits the pump to the rear of the control unit. Check that the tubing is secure.
D With the tubing set inserted, press the compartment downwards until it clicks into place.
SETUP
4 Insert the spike at the end of
the tubing set into the infil-
tration fluid bottle and hang
the bottle onto the stand.
5 Open the roller clamp on the
tubing set as far as it will go.
6 Open the vent valve at the
spike.
7 Connect the control unit to
the power socket.

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved
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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
OPERATION
CLEANING AND DISINFECTION
SWITCHING THE DEVICE ON AND OFF
The main switch «I/O» at the back of the unit is used to switch the control unit on and off. Switching off can be
done at any time and is not dependent on a switch-off procedure.
The green LED light at the top left of the control panel lights up when the main switch has been activated and
the unit is ready for operation.
REGULATION OF THE INFILTRATION PROCESS
Control dial in conjunction with ON/OFF foot switch The desired volumetric displacement is set with the
control dial. The pumping process is started by actuating the ON/OFF foot switch. The volumetric displace-
ment can be varied at any time using the control dial.
Control dial in conjunction with VARIO foot switch The maximum volumetric displacement can be varied
at any time using the control dial, even while the foot switch is being pressed. Control using the VARIO foot
switch regulates the volumetric displacement of the pump up to the set maximum value.
PERISTALTIC PUMP
Turn control dial clockwise from the OFF position. Pump starts, liquid emerges from the open tube end. Turning
the dial up to the maximum value controls the increase in volumetric displacement.
The pump stops immediately when the release button of the pump compartment is pressed.
FUNCTIONAL CHECK
Prior to DispenserDP30LipoPlus startup or use of accessory equipment, the user must always ensure that each
individual component is in good working order, free of defects, clean, sterile and operational. The tube set has to
correspond with the correct flow direction and the pump has to function. The green LED is on after the device is
switched on.
Clean and disinfect the devices after every treatment!
CONTROL UNIT AND FOOT SWITCH
Wipe the outside using tested surface disinfectant or 70% of isopropyl alcohol. The front plate of the control unit
is sealed and can be wiped clean.
TUBING SET REF6022
Single-use tubing sets may not be reused!
Used tubing sets must be disposed of properly.
Don’t use tube set when pack is already opened or damaged!
Do not use tubing set if expired.
Use only NOUVAG tubing sets with REF6022.
Sterility cannot be guaranteed by reusing and re-sterilization of tubing sets. The characteristics of the device
may change resulting in serious infections or, in worst case, the death of the patient.

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INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
MAINTENANCE
REPLACING THE CONTROL UNIT FUSES
Users can replace faulty control unit fuses themselves. These are located at the rear of the device in the fuse slot
beside the power switch:
1 Switch off device.
2 Unplug the power plug.
3 Open the fuse slot using a screwdriver.
4 Replace the faulty fuse T3,15 A, 250 V AC.
5 Slide the fuse holder back in and close the fuse slot.
6 Check the mains voltage shown on the fuse slot.
7 Plug in the power plug again.
1Fuse slot locking mechanism 2Display window for voltage setting 3Fuse slot 4Fuse1 5Fuse2
SAFETY INSPECTIONS
The essential requirements have been defined and assessed within the risk analysis. The results of the analysis
are stored in the risk management file of the manufacturer.
The performance of safety inspections on medical devices is required by law in several countries. The safety
inspection is a regular safety check that is compulsory for those operating medical devices. The objective is to
ensure that device defects and risks to patients, users or third parties are identified in time.
The STI (Safety Technical Inspection) for the DispenserDP30LipoPlus shall be executed every 2years by autho-
rized experts. Results shall be documented. The service manual, wiring diagrams, and descriptions are available
upon request from the manufacturer.
NOUVAG offers a safety inspection service for its customers. Addresses can be found in the appendix of this
instructions for use under S  >. For further information please contact our technical service
department.

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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
MALFUNCTIONS AND TROUBLESHOOTING
MALFUNCTION CAUSE SOLUTION REFER TO INSTRUCTIONS FOR USE
Device is
not functional
(Indicator
light is off)
Control unit not switched
on
Set the power switch « I/O »
to « I »
S      > 
Power connection not
established
Connect the control unit to
the mains power supply
C     >
Incorrect operating
voltage
Check the mains voltage C     >
Faulty fuse Replace fuse R     > 
Pump
doesn’t work
(Indicator
light is on)
Infiltration quantity set
too low or set to « OFF »
Raise pump performance by
turning control switch up
R     > 
Tubing set incorrectly
inserted
Insert tubing set correctly  D  > 
Incorrect operation Check instructions for use D  > 
Foot switch was not
pressed
Press foot switch down,
if infiltration process is
controlled via the foot switch
R     > 
Roller clamp is closed Open roller clamp all the
way
D  > 
Foot switch
doesn’t work
(Indicator
light is on)
Foot switch is not
connected
Connect foot switch with the
socket on rear of device
D  > 
D  > 
Incorrect operation Check instructions for use D  > 
R     > 
If the problem cannot be solved please contact your supplier or an authorized service center. Addresses can be found in the appendix of this instruc-
tions for use under S  >.

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 13
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
ACCESSORIES AND SPARE PARTS
ACCESSORIES
DESCRIPTION REF
ON/OFF foot switch 1527nou
VARIO foot switch 1511nou
Stand for irrigation fluid bottle 1770
Disposable tubing set, sterile, 4 m 6022
To order any additional parts, please contact our customer service department.
INFORMATION ON DISPOSAL
Electrical and electronic devices that have reached the end of their service life comprise hazardous waste
and may not be disposed of together with household waste. Prevailing national and local disposal regula-
tions apply.
When disposing of the device, device components and accessories, the requirements specified in legislation
must be followed. To ensure environmental protection, old devices can be returned to the dealer or manufac-
turer.
TECHNICAL DATA
Voltage, switchable 100 V~ / 115 V~ / 230 V~, 50 / 60 Hz
Fuse power supply 2 fuses, T 3,15
A, 250 V AC
Power consumption 120 VA
Volumetric displacement 1 – 24 l/h
Maximum pressure with closed tube set 2,0 bar
Applied part Type BF*
Protection class Class I
Dimensions (W x D x H) 260 x 250 x 110
mm
Net weight control unit 3,4 kg
Maximum weight at the stand for the irrigation fluid bottle 2,0 kg
The mentioned volumetric displacement is only valid for aqueous solutions without any instrument connected.
* Applied part is the tube set with its attached instruments.

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved
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DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
WARRANTY COVERAGE
NOUVAG warrants this product to be free from defects in workmanship and materials for a period of
twelve(12)months from the original date of purchase. If the warranty card is returned for registration or the
warranty extension is requested on our website within 4weeks from the date of purchase, the warranty coverage
is extended for a period of 6months, wear parts are excluded from the warranty. During this warranty period,
NOUVAG agrees to either repair or replace the product at its option if the product fails to function properly under
normal use and service and such failure is due solely to a defect in workmanship or materials.
This warranty is void if repair or service of the product is performed or attempted by anyone not authorized by
NOUVAG to do so, or if a replacement part not authorized by NOUVAG is used in any repair or service.
POST MARKET SURVEILLANCE
In the event of incidents related to the use of the medical device, please contact immediately the manufac-
turer by email [e-mail] or by phone.
To provide adequate information, please compile the incident questionnaire at the web address
Nouvag.com > Contact us > Incident questionnaire.
SERVICE POINTS
Switzerland
NOUVAGAG
St. Gallerstrasse 25
9403 Goldach
Phone [phone]
[email protected]om
www.nouvag.com
Germany
NOUVAGGmbH
Schulthaissstrasse 15
78462 Konstanz
Phone [phone]
info-[email protected]om
www.nouvag.com
A complete list of NOUVAG certified service points are found on the NOUVAG website: Nouvag.com > Service

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 15
Electromagnetic compatibility (EMC)
Remark:
The Product subsequently referred to herein always denotes the Dispenser DP 30 LipoPlus.
Changes or modifications to this product not expressly approved by the manufacturer may result in increased emissions or decreased immunity
performance of the product and could cause EMC issues with this or other equipment. This product is designed and tested to comply with
applicable regulations regarding EMC and shall be installed and put into service according to the EMC information stated as follows.
WARNING
Use of portable phones or other radio frequency (RF) emitting equipment, including accessories (antennas e.g.) in distances below
30 cm (12 inches) to the product, may cause unexpected or adverse operation.
WARNING
The product is suitable for use in hospitals other than in the vicinity of active devices of the HF surgical devices or except in HF
screening rooms used for magnetic resonance imaging.
WARNING
The product shall not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the product
shall be tested to verify normal operation in the configuration in which it is being used.
Essential Performance
The essential performance is that the infiltration of tumescent solution in the fat tissue taking into account the infiltration flow rate and pressure is
maintained. The maximum infiltration flow rate deviation is ± 25%, the infiltration flowrate is between 60 and 480ml/min and the maximum pressure
is 2.5bar.
Compliant Cables and Accessories
WARNING
The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity
performance of the product.
The table below lists cables, transducers, and other applicable accessories for which the manufacturer claims EMC compliance.
NOTE: Any supplied accessories that do not affect EMC compliance are not listed.
Description Length max.
Power supply cord REF 22261 / 22262 / 22264 / 22266 3.0m
Foot pedal IPX8 REF 1511nou / 1527nou 2.9m
Guidance and manufacturer’s declaration
–
electroma
g
netic emissions
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of the Product should
assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The Product uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B The Product is suitable for use in all establishments, including
domestic establishments and those directly connected to the
public low-voltage power supply network that supplies buildings
used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/flicker emissions
IEC 61000-3-3
complies
Guidance and manufacturer’s declaration
–
electromagnetic immunity
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of the Product should
assure that it is used in such an environment.
Immunity tests IEC 60601
Test level
Compliance level Electromagnetic environment - guidance
Electrostatic discharge
(ESD)
IEC 61000-4-2
+/- 8 kV contact
+/- 2 kV, +/- 4 kV, +/- 8 kV,
+/- 15 kV air
+/- 8 kV contact
+/- 2 kV, +/- 4 kV, +/- 8 kV,
+/- 15 kV air
Floors should be wood, concrete or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30 %.
Electrical fast
transient/burst
IEC 61000-4-4
+/- 2 kV with 100kHz
for power supply lines
+/- 1 kV with 100kHz
for input/output lines
+/- 2 kV with 100kHz
for power supply lines
+/- 1 kV with 100kHz
for input/output lines
Mains power quality should be that of a typical
commercial or hospital environment.
Surge
IEC 61000-4-5
+/- 0.5 kV, +/- 1 kV
differential mode
+/- 0.5 kV, +/- 1 kV, +/- 2 kV
common mode
+/- 0.5 kV, +/- 1 kV
differential mode
+/- 0.5 kV, +/- 1 kV, +/- 2 kV
common mode
Mains power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
0 % UT; for 0,5 cycle
with 0, 45, 90, 135, 180, 225,
270, 315 degree
0 % UT; for 1 cycle
0 % UT; for 0,5 cycle
with 0, 45, 90, 135, 180, 225,
270, 315 degree
0 % UT; for 1 cycle
Mains power quality should bet hat of a typical
commercial or hospital environment.
If the user of the Product requires continued
operation during power mains interruptions, it
is recommended that the Product be powered
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
APPENDIX

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved
16
Electromagnetic compatibility (EMC)
Remark:
The Product subsequently referred to herein always denotes the Dispenser DP 30 LipoPlus.
Changes or modifications to this product not expressly approved by the manufacturer may result in increased emissions or decreased immunity
performance of the product and could cause EMC issues with this or other equipment. This product is designed and tested to comply with
applicable regulations regarding EMC and shall be installed and put into service according to the EMC information stated as follows.
WARNING
Use of portable phones or other radio frequency (RF) emitting equipment, including accessories (antennas e.g.) in distances below
30 cm (12 inches) to the product, may cause unexpected or adverse operation.
WARNING
The product is suitable for use in hospitals other than in the vicinity of active devices of the HF surgical devices or except in HF
screening rooms used for magnetic resonance imaging.
WARNING
The product shall not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the product
shall be tested to verify normal operation in the configuration in which it is being used.
Essential Performance
The essential performance is that the infiltration of tumescent solution in the fat tissue taking into account the infiltration flow rate and pressure is
maintained. The maximum infiltration flow rate deviation is ± 25%, the infiltration flowrate is between 60 and 480ml/min and the maximum pressure
is 2.5bar.
Compliant Cables and Accessories
WARNING
The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity
performance of the product.
The table below lists cables, transducers, and other applicable accessories for which the manufacturer claims EMC compliance.
NOTE: Any supplied accessories that do not affect EMC compliance are not listed.
Description Length max.
Power supply cord REF 22261 / 22262 / 22264 / 22266 3.0m
Foot pedal IPX8 REF 1511nou / 1527nou 2.9m
Guidance and manufacturer’s declaration
–
electroma
g
netic emissions
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of the Product should
assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The Product uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B The Product is suitable for use in all establishments, including
domestic establishments and those directly connected to the
public low-voltage power supply network that supplies buildings
used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/flicker emissions
IEC 61000-3-3
complies
Guidance and manufacturer’s declaration
–
electromagnetic immunity
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of the Product should
assure that it is used in such an environment.
Immunity tests IEC 60601
Test level
Compliance level Electromagnetic environment - guidance
Electrostatic discharge
(ESD)
IEC 61000-4-2
+/- 8 kV contact
+/- 2 kV, +/- 4 kV, +/- 8 kV,
+/- 15 kV air
+/- 8 kV contact
+/- 2 kV, +/- 4 kV, +/- 8 kV,
+/- 15 kV air
Floors should be wood, concrete or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30 %.
Electrical fast
transient/burst
IEC 61000-4-4
+/- 2 kV with 100kHz
for power supply lines
+/- 1 kV with 100kHz
for input/output lines
+/- 2 kV with 100kHz
for power supply lines
+/- 1 kV with 100kHz
for input/output lines
Mains power quality should be that of a typical
commercial or hospital environment.
Surge
IEC 61000-4-5
+/- 0.5 kV, +/- 1 kV
differential mode
+/- 0.5 kV, +/- 1 kV, +/- 2 kV
common mode
+/- 0.5 kV, +/- 1 kV
differential mode
+/- 0.5 kV, +/- 1 kV, +/- 2 kV
common mode
Mains power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
0 % U
T;
for 0,5 cycle
with 0, 45, 90, 135, 180, 225,
270, 315 degree
0 % UT; for 1 cycle
0 % U
T;
for 0,5 cycle
with 0, 45, 90, 135, 180, 225,
270, 315 degree
0 % UT; for 1 cycle
Mains power quality should bet hat of a typical
commercial or hospital environment.
If the user of the Product requires continued
operation during power mains interruptions, it
is recommended that the Product be powered
70 % U
T
; for 25/30 cycles
0 % UT; for 5 sec
70 % U
T
; for 25/30 cycles
0 % UT; for 5 sec
from an uninterruptible power supply or a
battery.
Power frequency
(50/60Hz) magnetic field
IEC 61000-4-8
30 A/m 30 A/m Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
Note: UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration
–
electromagnetic immunity for not life support equipment
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of the Product should
assure that it is used in such an environment.
Immunity tests IEC 60601
Test level
Compliance level Electromagnetic environment - guidance
Portable and mobile RF communications
equipment should be used no closer to any part
of the Product, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency of
the transmitter.
Recommended separation distance:
Conducted RF
IEC 61000-4-6
3 V rms
0.15 MHz to 80 MHz
6 V rms
inside ISM bands between
150 kHz to 80 MHz
80% AM bei 1 kHz
3 V rms
0.15 MHz to 80 MHz
6 V rms
inside ISM bands between
150 kHz to 80 MHz
80% AM bei 1 kHz
d = 0,35 P
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to 2.7 GHz
80% AM bei 1 kHz
3 V/m
80 MHz to 2.7 GHz
80% AM bei 1 kHz
d = 0,35 P 80 MHz to 800 MHz
d = 0,7 P 800 MHz to 2,7 GHz
Where P is the maximum output power rating in
the transmitter in watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance in metres
(m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey a,
should be less than the compliance level in each
frequency range b.
Interference may occur in the vicinity of
equipment marked with the following symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
a Fixed strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To access the
electromagnetic environment due to fixed RF transmitters, and electromagnetic site survey should be considered. If the
measured field strength in the location in which the Product is used exceeds the applicable RF compliance level above, the
Product should b observed to verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the Product.
b over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
DISPENSERDP30LIPOPLUS INSTRUCTIONS FOR USE
APPENDIX

©NOUVAGAG • 31628 • V20230301 • Allrightsreserved 17
Electromagnetic immunity against high-frequency wireless communication devices
Test frequenc
y
MHz
Frequency
band
MHz
Communication
service
Modulation Maximum
Performance
W
distance
m
Test level
V/m
385 380 to 390 TETRA 400 Pulse modulation
18 Hz 1.8 0.3 27
450 430 to 470 GMRS 460,
FRS 460
FM
± 5 kHz Hub
1 kHz Sinus
2 0.3 28
710
704 to 787 LTE Band 13, 17 Pulse modulation
217 Hz 0.2 0.3 9
745
780
810
800 to 960
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse modulation
18 Hz 2 0.3 28
870
930
1720
1700 to 1990
GSM 1800,
CDMA 1900,
GSM 1900,
DECT,
LTE Band 1, 3,
4, 25; UMTS
Pulse modulation
217 Hz 2 0.3 28
1845
1970
2450 2400 to 2570
Bluetooth,
WLAN 802.11
b/g/n,
RFID 2450,
LTE Band 7
Pulse modulation
217 Hz 2 0.3 28
5240
5100 to 5800 WLAN 802.11 a/n Pulse modulation
217 Hz 0.2 0.3 9 5500
8785
Recommended separation distances between
portable and mobile RF communications equipment and the not life support equipment
The Product is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the
user of the Product can help prevent electromagnet interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the Product as recommended below, according to the maximum output power of the
communications equipment.
Rated maximum output power
of transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d = 0,35 P
80 MHz to 800 MHz
d = 0,35 P
800 MHz to 2.5 GHz
d = 0,7 P
0,01 0,04 0,04 0,07
0,1 0,11 0,11 0,22
1 0,35 0,35 0,7
10 1,1 1,1 2,2
100 3,5 3,5 7
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be
estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter
in watts (W) according to the higher frequency range applies.
Note 1: At 80 MHz and 800 MHz, the separation distance fort the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
INSTRUCTIONS FOR USE DISPENSERDP30LIPOPLUS
APPENDIX

©NOUVAG AG • 31628 • V20230301 • All rights reserved
NOUVAGAG
St. Gallerstrasse 25
9403 Goldach
Switzerland
Phone [phone]
[email protected]om
www.nouvag.com
NOUVAGGmbH
Schulthaissstrasse 15
78462 Konstanz
Germany
Phone [phone]
info-[email protected]om
www.nouvag.com