Mantis MR991 Operation instructions
Via Artigianale Croce n.13 - 42035 Castelnovo ne’ Monti (RE) - ITALY
Tel. +39.0522.612080 - Tel./Fax +39.0522.729796
Integrated treatment system with endodermic massage
and application of pulsed magnetic fields with stochastic resonance
MR991
Use and Maintenance Instructions
The manual must be kept in a safe place for the entire life of the machine. Please read carefully the
manual before operating any part of the equipment
Includes CE Certificate of Conformity
INDEX
DECLARATION OF CONFORMITY CE ........................................................................ 4
1 GENERAL INFORMATION ................................................................................. 5
1.1 Equipment description.................................................................................... 5
1.2 Definitions and symbols used in the manual ................................................ 5
2 SCOPE.................................................................................................................. 6
2.1 Intended use................................................................................................... 6
2.2 Reasonably foreseeable misuse .................................................................. 6
3 TECHNICAL DATA ................................................................................................ 8
4 EQUIPMENT DESCRIPTION .............................................................................. 9
4.1 Equipment ...................................................................................................... 9
4.2 Handpieces ...................................................................................................11
5 GENERAL SAFETY PRECAUTIONS ............................................................... 12
5.1 Instructions ................................................................................................ 12
5.2 Safety devices ............................................................................................. 13
5.3 Pictograms ................................................................................................ 14
6 TRANSPORT AND INSTALLATION .................................................................. 15
6.1 Description of the package and storage...................................................... 15
6.2 Removal of package and content check ................................................... 14
6.3 Transport ................................................................................................... 15
6.4 Installation ................................................................................................... 15
6.4.1 Positioning................................................................................................ 15
6.4.2 Assembly ................................................................................................ 16
6.4.3 Power connection .................................................................................... 17
6.4.4 Connection for telecare (if available) ...................................................... 18
7 COMMISSIONING ............................................................................................. 19
7.1 Equipment functions.................................................................................... 19
7.1.1 Maxi DES handpiece................................................................................. 19
7.1.2 Mini DES handpiece ................................................................................. 19
7.1.3 Maxenergy handpiece .............................................................................. 19
7.1.4 Vixo handpiece.......................................................................................... 19
7.2 Switching on and preparation of the equipment .......................................... 19
7.3 Start a treatment cycle .............................................................................. 22
7.3.1 Background information ........................................................................... 22
7.3.2 First treatment cycle ................................................................................. 22
7.3.3 Function control buttons on the handpieces (see 4.2 Handpieces) ......... 25
7.4 Repeat a treatment cycle ........................................................................... 25
7.5 Interruption of the ongoing treatment ......................................................... 27
7.6 Equipment emergency stop ........................................................................ 27
7.7 Equipment recovery in case of emergency ................................................ 27
7.8 Recovery from power failure ..................................................................... 27
8 EQUIPMENT MAINTENANCE........................................................................... 28
8.1 Routine maintenance .............................................................................. 28
8.1.1 Cleaning and disinfection of the handpieces .......................................... 28
8.1.2 Equipment cleaning ................................................................................. 28
8.1.3 Vacuum filters cleaning and cartridge replacement ................................. 29
2
3
9 ACCESSORIES AND OPTIONAL ITEMS ......................................................... 30
9.1 Accessories ............................................................................................. 30
9.2 Installation of accessories ........................................................................ 30
9.2.1 Handpiece without PMF system – Code MN50043 ................................. 30
10 EQUIPMENT DECOMISSIONING ..................................................................... 31
11 PROBLEMS AND SOLUTIONS ........................................................................ 31
12 SPARE PARTS................................................................................................... 32
13 GENERAL WARRANTY TERMS AND CONDITIONS ....................................... 33
DECLARATION OF CONFORMITY
MANTIS S.R.L.
Via Artigianale Croce n.13 - 42035 Castelnovo ne’ Monti (RE) - ITALY
Tel. +39.0522.612080 - Tel./Fax +39.0522.729796
declares under its sole responsibility that the equipment
Type: Integrated treatment system with endodermic massage and application
of pulsed magnetic fields with stochastic resonance
Model: MR991
Serial number: ................................
Year of manufacture: ................
complies with all relevant provisions of:
Directive 2001/95/EC and subsequent amendments and additions;
Legislative Decree no. 110 of 12 May 2011 and subsequent amendments;
also complies with the following directives:
- 2004/108/CE Electromagnetic compatibility
- 2006/95/CE Low voltage
complies with the following regulations:
- CEI 62-39 Electrical equipment for the beauty industry - General safety guide
- CEI EN 60601-1 third edition and subsequent amendments
Electromedical equipment Part 1: General requirements for basic safety
and essential performance
The manufacturer also declares that the technical construction file is kept at: MANTIS S.R.L. Via
Artigianale Croce 13 - 42035 Castelnovo ne’ Monti (RE) - Italy
Castelnovo ne’ Monti (RE), ........
Cristian Rossi
Technical Manager
Mantis S.r.l.
4
5
1 GENERAL INFORMATION
1.1 Equipment description
MR991 is a machine intended for beauty operators and designed to improve body and face
appearance.
The MR991 system combines two technologies which can be easily programmed by the operator:
- the MRM (mechanical manipulation with motorised rollers) which carries out an endodermic
massage thanks to the mechanical movement of rollers and the microsuction.
- the CMPS SYSTEM (pulsed magnetic fields with stochastic resonance). Tests show that parts
treated with CMPS have a greater blood supply than usual, thus leading to a greater oxygen
exchange to the tissue and at the same time draining all toxic and unwanted substances
towards the organs of detoxification and excretion. Thanks to its detoxifying action, which drains
the stagnant liquid in the tissue, the CMPS system is ideal to treat lymphoedema and cellulite.
1.2 Definitions and symbols used in the manual
The manual includes some pictures which have been defined and authorised for use on the
equipment according to different purposes:
Manufacturer: the equipment producer who affixes his own distinctive brand on the equipment
(MANTIS s.r.l.).
Operator: the personnel who operate the equipment and have practical knowledge of its
functioning following a training course providing the relevant qualification issued by the
manufacturer. The operator is also in charge of the cleaning and routine maintenance of the
equipment.
Customer: the person being treated or asking for a treatment.
Technical Assistance: the personnel specifically assigned by the manufacturer for emergency
maintenance and repair services on the equipment.
The following symbols are used in the manual:
Safety requirements
Use and maintenance requirements
2 SCOPE
2.1 Intended use
MR991 is designed for face and body beauty treatment which is carried out with special
handpieces driven by a software that also guides the operator throughout the entire treatment.
A “checkup” form on the Customer’s general state of health is previously filled in to evaluate any
risk factors which could lead to the exclusion of some treatment phases.
Each handpiece is intended for a specific type of treatment, namely:
- MAXI DES (MRM + programmable CMPS SYSTEM): suitable for body treatment on the
recommended areas and following the specified procedure;
- MINI DES (MRM + programmable CMPS SYSTEM): suitable for body treatment on the
recommended areas and following the specified procedure;
- MAXENERGY (CMPS SYSTEM for application of cream treatment): suitable for body treatment
on the recommended areas and following the specified procedure;
- VIXO (programmable CMPS SYSTEM + microsuction): suitable for face treatment on the
recommended areas and following the specified procedure.
2.2 Reasonably foreseeable misuse
MR991 (in any of its functions) should not be used in the following cases:
- People with implantable devices (heart stimulators, internal defibrillators, etc.)
- Treatment on open wounds, eyes, body cavities, nipples and testicles.
MR991 in MRM mode (mechanical manipulation with motorised rollers) should not be used
in the following cases:
- Thrombophlebitis
- Cardiocirculatory insufficiency
- Phlebitis
- Dermatological infections
- Hypertension
- Varicose veins
- Skin cancers (neoplasias)
- Tuberculosis
MR991 in CMPS SYSTEM mode (pulsed magnetic fields with stochastic resonance) should
not be used in the following cases:
- Presence of metal prostheses such as implant screws, staples, nails, clips, etc.
- Heart rhythm disorders
- Dermatitis
- Epilepsy
- Disorders of the autonomic nervous system
- Nervous disorders
- Pregnancy
- Menstrual cycle with heavy bleeding
- Open haemorrhoids and vascular lesions in general
- People with intrauterine devices such as catheter, coil, etc.
- Localised fungal infections
- Fever or disorders of thermoregulation
6
With the exception of the above-mentioned cases, in the following cases MR991 (in any of
its functions) must be used carefully and only with the doctor’s approval:
- Pregnancy
- Asthma
- Tumours (neoplasias)
- Scleropathy
- Lymphopathy
- Mesotherapy
- Psoriasis
- Multiple sclerosis
- Scleroderma
Before starting the treatment, the Customer should be thoroughly informed
about all the treatment contraindications. All fields in the “checkup” form
must be filled in, including date and signature. Make sure that during the
treatment cycle the Customer’s health conditions do not undergo any change,
which could be a contraindication for the treatment.
Under no circumstances should MR991 be used to treat people with
implantable devices (heart stimulators, internal defibrillators, etc.).
Under no circumstances should MR991 be used to treat open wounds, eyes,
body cavities, nipples and testicles.
The Manufacturer will assume no responsibility if maintenance is not carried
out in the manner and within the time prescribed (see par. 8 EQUIPMENT
MAINTENANCE).
The Manufacturer will assume no responsibility in the event of any tampering
or modification to the equipment carried out without the manufacturer’s prior
approval.
7
3 TECHNICAL DATA
8
H
P
L
MR 991
Width (W)
600 mm (23.62 in)
Depth (D)
600 mm (23.62 in)
Height (H)
1,950 mm (76.77 in)
Weight
110 Kg (242 lbs)
Minimum working space required around the
equipment
900 mm (35.43 in)
Power cable length
2.5 m (8.2 ft)
Working length of handpiece tubes
2 m (6.5 ft)
Degree of protection
IP20
Degree of protection against direct and indirect
contact
BF type
Insulation class
1
Power supply
230 V - 2P+E
Frequency
50÷60 Hz
Circuit breaker
10 A
Maximum power consumption
1200 W
4 EQUIPMENT DESCRIPTION
4.1 Equipment
1 Touch-screen control panel
2 Vixo handpiece
3 Maxi DES handpiece
4 Mini DES handpiece
5 Maxenergy handpiece
6 Key switch
7 Emergency stop
8 USB port
9 Wheels
10 Wheels with brake system
11 Carrying handles
9
2
3
1
4
5
67
10
9
9
8
11 11
2 Vixo handpiece
3 Maxi DES handpiece
4 Mini DES handpiece
5 Maxenergy handpiece
21 Transparent handpiece holder
22 Cable conduit cover
23 Handpiece connector cover
24 Ethernet connection
25 Main switch
26 Maxenergy connection
27 Electric power supply
28 Mini DES / Maxi DES connections
29 Mini DES / Maxi DES connections
30 Vixo connections
31 Filters
10
21
22
23
24 26
25
27
4
3
2
5
30
28 29
31
23
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