Gima GIMA MAMILAT User guide

TIRALATTE NEW MAMILAT

NEW MAMILAT BREAST - PUMP

TIRE – LAIT NEW MAMILAT
MILCHPUMP NEW MAMILAT
MAMADERA NEW MAMILAT

MANUALE D’USO

USER MANUAL

MODE D’EMPLOI

NEW MAMILAT è una pompa a depressione, ad alimentazione elettrica 230V~, da utilizzarsi per il prelievo di latte
materno dal seno. Particolarmente adatto per l’impiego ospedaliero in reparti di maternità e / o per l’impiego a domicilio.
Dispositivo progettato per offrire facilità di trasporto e impiego non continuo.

M28148 –M-Rev.4.10.07

GIMA S.p.A. – Via Monza, 102 – 20060 Gessate (MI) – Italia

INTERNATIONAL: Tel. [phone]/221/225 – Fax. [phone]

MANUAL DE ISTRUCCIONES

ITALIA: Tel. [phone] – Fax. [phone]

e-mail: [e-mail]

e-mail: [e-mail]

HANDBUCH

– www.gimaitaly.com

– www.gimaitaly.com

NEW MAMILAT breast pump : it’s a device working with 230V~ / 50 Hz network electricity equipped with a low
pressure pump. The device was made for the aspiration of the maternal milk.
Easily transportable from one maternity ward to another, or for use at home.
To be used for aspirating mother's milk.
Easily portable equipment designed for virtually not continuous use 20 min ON / 40 min. OFF.
Made of highly heat-resistant, electrically insulated plastic material in conformity with the latest European
safety standards.
Supplied with two polycarbonate biberon 250cc complete with teats and nipple shields.
Equipped with aspiration regulator, located on the front panel.

GENERAL WARNING

READ INSTRUCTION MANUAL CAREFULLY BEFORE USE

ONLY HIGHLY QUALIFIED STAFF USE RESERVED

THE INSTRUMENT MUST NOT BE DISASSEMBLED
FOR A TECHNICAL SERVICE ALWAYS CONTACT GIMA S.p.A.

IMPORTANT SAFETY RULES

1. On opening the packaging, check the integrity of the appliance, paying particular attention to the presence of
damage to the plastic parts, which may make access possible to internal live parts and also to breakage and / or
peeling of the power supply cable. In these cases don’t connect the plug to the electric socket.
Carry out these controls before each use;

2. before connecting the appliance always check that the electric data indicated on the data label and the type of
plug used, correspond to those of the mains electricity to witch it’s to be connected;

3. If the plug supplied with the appliance is incompatible with the mains electricity socket, contact qualified staff for
replacement of the plug with a suitable type. The use of simple or multiple and / or extension adapters is not
generally recommended. Whenever their use is indispensable, use those in compliance with safety regulations,
however paying attention not to exceed the maximum power supply limits, which are indicated on the adapters
and extensions;

4. Respect the safety regulations indicated for electrical appliances and particularly:

• Only use original accessories and components;

• The device can be used only with the bacteriological filter;

• Never immerge the appliance into water;

• Position the appliance on flat stable surfaces;

• Position the device in a way that the air inlets on the back aren’t obstructed;

• Never use the device in environments which have anaesthetic mixtures inflammable with air, oxygen or

nitric oxide;

• Don’t touch the device with wet hands and always prevent the appliance coming into contact with liquids;

• Keep off the reach of children or not capable people without supervision;

• Don’t leave the appliance connected to the power supply socket when not in use;

• Don’t pull the power supply cable to disconnect the plug remove the plug from the mains socket correctly;

• Preserve and use the medical device in environments protected from atmospheric factors and at a

5. For repairs, exclusively contact GIMA S.p.A. technical service and request the use of original spare parts.

6. This medical device must be destined exclusively for the use for witch it has been designed ad

7. Particular precautions must be made concerning electromagnetic compatibility. The medical device must be

8. Instrument and accessories discharging must be done following current law regulations in every country of use.

distance from heat sources;

Failure to comply with the above can jeopardise the safety of the device;

described in this manual. Any different use must be considered incorrect and therefore dangerous; the
manufacturer cannot be considered liable for damage caused by improper, incorrect and / or unreasonable use
or if the appliance is used in electrical plants that are not in compliance with the regulations in force;

installed and used according to information supplied with the accompanying documents;

8

TYPOLOGY (MDD 93/42/EEC) Dispositivo Medico Classe IIa
MODEL
UNI EN ISO 10079-1 HIGH VACUUM / LOW FLOW
POWER FEEDING 230V~ / 50Hz 110V~ / 60Hz

POWER CONSUMPTION 184VA 105VA
FUSE F 1 x 1.6A 250V F 1 x 4A 250V
MAXIMUM SUCTION PRESSURE (without jar) -33kPa (-0.33 bar)
MAXIMUM SUCTION FLOW (without jar) 14 l/min
WEIGHT 2.2 Kg
SIZE 235 x 190 x 165 mm
DUTY CYCLE
(to 35°C and 110% operating voltage)
WORKING CONDITION

CONSERVATION CONDITION AND TRASPORT

Room temperature: 10 ÷ 40°C
Room humidity percentage: 20 ÷ 85% RH
Altitude: 0 ÷ 2000m s.l.m.
Room temperature: -40÷ 70°C
Room humidity percentage: 10 ÷ 95% RH

NEW MAMILAT

(no CE 0123)

20 min ON / 40 min OFF

SYMBOLS

TECHNICAL CHARACTERISTICS

Class II isolation equipment

~

Hz

O

I

CE marking in conformity with EC directive 93/42/EEC

Manufactured by: CA.MI. di Attolini Mario & C. s.n.c.

Via Ugo La Malfa n° 31 - 43010 Pilastro (PR) Italia

Warning, consult the instruction manual

To Preserve in place coolness and dry land

Conservation temperature: -40 ÷ 70°C

Type B equipment

Fuse

Alternate Current
Mains Frequency

ON

OFF

9

Guidance and manufacturer’s declaration – Electromagnetic Emissions

The Breast-Pump NEW MAMILAT is intended for use in the electromagnetic environment specified below.

The customers or the user of the Breast-Pump NEW MAMILAT should assure that it’s used in such an

Emissions Test Compliance Electromagnetic environment -

Irradiated / Conducted emissions
CISPR11

Irradiated / Conducted emissions
CISPR11
Harmonic emissions
IEC/EN 61000-3-2
Voltage fluctuations /
flicker emissions
IEC/EN 61000-3-3

The Breast-Pump NEW MAMILAT is intended for use in the electromagnetic environment specified below.

The customers or the user of the Breast-Pump NEW MAMILAT should assure that it’s used in such an

Guidance and manufacturer’s declaration – Electromagnetic Emissions

Immunity Test Compliance Electromagnetic environments -

Electrostatic discharge (ESD)

IEC/EN 61000-4-2

Electrical fast transient / burst

IEC/EN 61000-4-4

Surge

IEC/EN 61000-4-5

Loss of voltage, brief voltage

interruptions and variations

IEC/EN 61000-4-11

Magnetic field

IEC/EN 61000-4-8

Conducted Immunity

IEC/EN 61000-4-6

Irradiated Conducted

IEC/EN 61000-4-3

Note UT is the value of the power supply voltage

(as request by regulation EN 60601-1-2:2001)

environment.

Group 1

Class [B]

Class [A]

Complies

The Breast-Pump NEW MAMILAT only
used RF energy only for its internal
functioning.
Therefore its RF emissions are very low
and are not cause interference in
proximity of any Electronic appliances.
The Breast-Pump NEW MAMILAT can
be used in all environments, including
domestic and those connected directly
to the public mains distribution that
supplies power to environments used
for domestic scopes.

(as request by regulation EN 60601-1-2:2001)

environment.

± 6kV on contact

± 8kV in air

± 2kV power supply

± 1kV differential mode

5%UT for 0.5 cycle

40%U

for 05 cycle

T

70%U

for 25 cycle

T

<5%U

T

for 5 sec

3A/m

3Vrms 150kHz to 80MHz

(for appliances that aren’t life -

supporting)

3V/m 80MHz to 2.5 GHz

(for appliances that aren’t life -

equipment)

Floors should be wood, conceret or
ceramic tile. If floors are coverei with
synthetic material, the relative
humidity should be at least 30%.
Mains power quality should be that of a
typical commercial environment or
hospital
Mains power quality should be that of a
typical commercial environment or
hospital
Mains power quality should be that of a
typical commercial environment or
hospital If the user of Breast-Pump
NEW MAMILAT request that the
appliance operates continuosly, the
use of a continuity unit is
recommended.
The power frequency magnetic field
should be measured in the intended
installation location to assure that it’s
sufficiently low.

guidance

guidance

-

-

10

The filter is produced with (PTFE) hydrophobic material witch prevents fluids entering the pneumatic
circuit. When the filter is wet, it’s not possible to use the unit therefore the filter should be changed
immediately.
In case of possible contamination or discolouration, change the filter immediately.
Don’t use the suction unit without the protection filter fitted. If the suction unit is used in an emergency
or in a patient where the risk of contamination is not know the filter must be changed after each use.

DESCRIPTION

Nipple shield
PC milk biberon 250cc
PC milk biberon 125cc

Nebulizer air Tube with connectors

Milk biberon security plug

Antibacterial Filter

CLEANING OF ACCESSORIES

To clean the instrument it is recommended to use a soft and dry cloth with not abrasive and not
solvent cleaning substances.
To disinfect accessories follow directions:

1. Grip the biberon with your hand and turn the cap in a counter - clockwise direction remove
the cap from the bottle.

2. Put the two biberons and the two caps into a suitable disinfectant solution

3. Disinfect accessories with methylated spirits or hypochlorite-based solutions, easily

ACCESSORIES SUPPLIED

The two aspiration tubes can be sterilized on autoclave using a sterilization cycle.

findable in chemist

DO NOT LEAVE INTERNAL PARTS COME IN CONTACT WITH LIQUIDS

DO NOT BOIL OR PUT IN AUTOCLAVE THE ACCESSORIES

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MAINTENANCE

The NEW MAMILAT breast pump does not need maintenance or lubrication.
It is necessary to check functioning and instrument before every use. Unpack the instrument and
always check integrity of plastic parts and feeding cable, they might have been damaged during
previous use. Connect cable to electrical network and turn switch on.
Close the aspirator outlet with your finger and with suction regulator in maximum vacuum position
check that the vacuum power.
Rotate the knob from right to left and check the aspiration regulating control.
The vacuum power should go down to the minimum value.
Verify that loud noises are not present, these can indicate wrong functioning.
A protection fuse (F 1.6 A 250V and F 4 A 250 V for voltage 110 V / 60 Hz) not reachable from
exterior protects the instrument.
For fuse replacing please contact GIMA S.p.A. technical assistance.

Fault type Cause Solution

1. No aspiration Bottle cap badly screwed

2. No aspiration Cap seal not in its seat Unscrew the cap and insert the seal

3. No aspiration due to
outflowing of milk from
overflow bottle

4. The motor doesn’t
work (green light on the
power switch on)

Faults 1 - 2 - 3 - 4 None of the remedies has

If the overfill security system it’s activated don’t proceed with the liquid aspiration.
The bacteriological filter will be stopped the aspiration.
If both the security system doesn’t work, there is the possibility that the liquid comes inside the device,
in this case return the device to CA-MI technical service.

down

Filter blocked Replace filter

Activation of the thermal

protection on the motor

achieved the desired

results

Unscrew the cap, then rescrew it correctly

properly in its seal

Wait for some times to avoid the

deactivation of the thermal protection,

after that the motor start again to work

Contact the seller or GIMA S.p.A. After-

sales Assistance Service

BEFORE EVERY CHECKING OPERATION, IN CASE OF ANOMALIES OR BAD FUNCTIONING,

PLEASE CONTACT GIMA S.p.A. TECHNICAL SERVICE.

GIMA S.p.A. DOES NOT GIVE GUARANTEE IF INSTRUMENT, AFTER THE TECHNICAL

SERVICE CHECKING, APPEARS TO BE TAMPERED.

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INSTRUCTIONS

• Connect the short silicon tube 1 to the filter 2 to one of the two outlets of the bottle 3

• The other end of the tube must be connected to the suction outlet of the equipment 4

• Connect the PVC air tube 6 to the other outlet of the bottle 5 (biberon 250cc)

• The other end of the tube must be connected to the small-diameter outlet of the breast pump

nipple shield located on the bottle.

• Connect the plug to the electrical mains supply.

• Switch on the equipment 7 to start suction and close the nipple shield's large-diameter outlet

with your finger

• The bottle without couple must be used as an overflow container. It must not be filled.

• The device must be used on a plan of horizontal operation.

IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE

At the end of its working life, the product must not be disposed of as urban waste.
It must be taken a special local authority differentiated waste collection or to a dealer providing this service.
Disposing of a household appliance separately avoids possible negative consequences for the environment
and health deriving from inappropriate disposal and enables the constituent materials to be recovered to
obtain significant saving in energy and resources. As a reminder of the need to dispose of separately the
product is marked with a crossed-out wheeled dustbin.

WITH EC DIRECTIVE 2002/96/EC:

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Montaggio Filtro / Filter Assembling
Mod: TOBI UNO / TOBI / SUPER TOBI / TOBI MANUALE / NEW MAMILAT /
SUPER TOBI BATTERIA / SUPER VEGA / VEGA / SUPER VEGA BATTERIA
(Cod. 28229)

DIREZIONE FLUSSO / FLOW DIRECTION

Connessione apparecchio /

Suction pump Inlet

IN / Fluid Inside

Montaggio Filtro / Filter Assembling
Mod: TOBI CLINIC / SUPER TOBI CARRELLATO (Cod. 28239)

TOBI HOSPITAL / TOBI HOSPI PLUS (Cod. 28237)

Connessione apparecchio

Suction Pump inlet

DIREZIONE FLUSSO / FLOW DIRECTION

Connessione Vaso /

Jar Air Tube

IN

Connessione Vaso

Jar Air Tube

32