Open Telematic Procedure for the supply of Electromedical Equipment to be allocated to the Hospitals and Health Districts of the Salerno ASL. Project "Por Campania Fesr 2014-2020 - Axis 1 - Specific objective 1.6 - Action 1.6.1. Intervention "Territorial and hospital strengthening of the Critical Area and time-dependent networks" – Cup C59I23000260002, and any other funding.

Rotary closed-loop anesthesia system suitable for addressing high anesthesiology procedures

Flows and low flows.

GENERAL CHARACTERISTICS

Latest generation compressed gas lung ventilator for use in intensive care

Able to deliver invasive and non-invasive ventilation

Intended for adult and paediatric patients

Scalable with high modularity, both hardware and software

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with suitable humidification system preferably active and preferable regulation

flow temperature

Sensor for O2 measurement preferably paramagnetic (or equivalent inexhaustible technology)

and integrated into the pneumatic body of the device

Equipped with adequate pre-operational tests such as leak tests and sensor calibration

Supplied and installed on a support trolley with antistatic wheels, swivel and equipped with

appropriate locking system and complete with pipe support arm

Mains power and built-in rechargeable battery to ensure operation for

at least 30min (not standby)

GENERAL CHARACTERISTICS

Latest generation compressed gas lung ventilator for use in intensive care

Able to deliver invasive and non-invasive ventilation

Intended for adult and paediatric patients

Scalable with high modularity, both hardware and software

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with suitable humidification system

Sensor for O2 measurement preferably paramagnetic (or equivalent inexhaustible technology)

and integrated into the pneumatic body of the device

Equipped with adequate pre-operational tests such as leak tests and sensor calibration

Supplied and installed on a support trolley with antistatic wheels, swivel and equipped with

appropriate locking system and complete with pipe support arm

Mains power and built-in rechargeable battery to ensure operation for

at least 30min (not standby)

GENERAL CHARACTERISTICS

Latest generation turbine lung ventilator for use in semi-intensive care

Able to deliver non-invasive ventilation

Intended for adult and paediatric patients

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with suitable humidification system

Supplied and installed on a support trolley with antistatic wheels, swivel and equipped with

appropriate locking system and complete with pipe support arm

Mains power and built-in rechargeable battery to ensure operation for

at least 30min (not standby)

Large color display

Simple, intuitive, menu-reduced and ergonomic user interface

Contemporary waveforms viewable on the screen: at least n.2 respiratory parameters (P, F, V)

over time

GENERAL CHARACTERISTICS

Latest generation compressed gas lung ventilator for use in intensive care

neonatal

Intended for paediatric and neonatal patients

Able to deliver invasive and non-invasive ventilation

Scalable with high modularity, both hardware and software

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with a suitable humidification system with the possibility of humidification regulation and

flow temperature (both invasive and NIV mode)

Adequate sensors for proximal flow detection

Integrated air/O2 mixer

Sensor for O2 measurement preferably paramagnetic (or equivalent inexhaustible technology)

and integrated into the pneumatic body of the device

Equipped with adequate pre-operational tests such as leak tests and sensor calibration

Supplied and installed on a support trolley with antistatic wheels, swivel and equipped with

appropriate locking system and complete with pipe support arm

Mains power and built-in rechargeable battery to ensure operation for

at least 30min (not standby)

GENERAL CHARACTERISTICS

Latest generation pulmonary ventilator for use in neonatal intensive care

Intended for neonatal patients

Able to deliver non-invasive nasal ventilation

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with suitable humidification system

Adequate sensors for flow detection

Supplied and installed on a support trolley with antistatic wheels, swivel and equipped with

appropriate locking system and complete with pipe support arm

Mains power and built-in rechargeable battery to ensure operation for

at least 30min (not standby)

GENERAL CHARACTERISTICS

Pulmonary ventilator for intra and extra-hospital transport with therapy characteristics

intensive and suitable for use also in ambulance

Able to deliver invasive and non-invasive ventilation

Intended for adult and paediatric patients

Of limited weight and size such as to easily allow sanitization operations and

handling

Equipped with appropriate devices (e.g. handles, straps, etc.) to simplify the operation of

handling, positioning and transport

Able to supply O2 from centralized system or cylinder

Equipped with adequate pre-operational tests such as leak tests and sensor calibration

Mains and integrated rechargeable battery power supply that ensures operation for

at least 2 hours (not standby)

Complete with carrying bag, supports for fixing in ambulance, stretcher and wall bar

WEARABLE MONITOR

Multi-parameter monitoring device in compact or modular configuration (in case of

modular system modules must be interconnected with each other)

Real-time and continuous monitoring of at least the following physiological parameters:

• ECG on at least 3 sampling points

• Heart rate

• NIBP

• SpO2

Small size and weight such as to make the device "wearable"

Powered by long-lasting rechargeable batteries

"Wireless" communication interface (Wifi, bluetooth, etc.) for the transmission of

Recorded data

"Buffer" type memory that allows parameters to be recorded even in the absence of

Communication

Complete with case / shoulder strap to comfortably wear the device and parts attached (cables and

sensors) necessary for the detection of all the parameters subject to monitoring

CE marking in accordance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

• Suitable for washing and thermodisinfection of surgical instruments, anesthesia material and

hooves

• Free installation

• Stainless steel washing chamber with a capacity of not less than 140 liters

• Ability to set predefined programs

• Display for displaying the set parameters, the washing phases and any messages

• Intuitive and easy-to-use control panel for program selection

• Equipped with electric hot air drying system (dryer)

• Equipped with acoustic/visual alarm systems

• Equipped with pumps for automatic dosing of at least detergent and neutralizer

• Dedicated compartment for the non-visible positioning of the jerry cans

• Equipped with serial interface for connection to external devices

• Equipped with printer for the traceability of operations

• Power supply 220V or 380V three-phase

• The equipment offered must be equipped with at least the following accessories:

Lower and upper basket kit/complete trolley/inserts for material positioning

laparoscopic surgery and surgery

Lower and upper basket kit/complete trolley/inserts for material positioning

anaesthesia

Lower and upper basket kit/complete trolley/inserts for the positioning of plinths

• The supply must include water softener (in addition to the system

possibly integrated) with flow rate and pressure adequately sized to serve the

Washer above

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

• Ultrasonic tank dedicated to the washing of surgical instruments

• Tank capacity not less than 20 liters

• Control panel with digital display for setting and displaying

operation

• Inner chamber made of corrosion-resistant material

• External structure made of chemical-resistant material

• Maximum operating temperature not lower than 60°C

• Adjustable washing time at least up to 30 minutes

• Complete with:

dedicated lid

removable perforated basket inside stainless steel

Starter kit of dedicated disinfectant material

• Mains power

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

EMERGENCY TROLLEY, PORTABLE MEDICAL SURGICAL ASPIRATOR, BLADE LARYNGOSCOPE SET, DEFIBRILLATOR, BENCHTOP PULSE OXIMETER. The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

equipment listed above (any connection cables, power cables, interface cables, battery chargers, adapters, patient cables, cc.) and any consumables / tests for the execution of the acceptance tests.

Apparatus intended for sterilization of surgical instruments at low temperature

• Radio frequency generator

• Suitable for urological interventions (such as transurethral resection in saline,

endoscopic resection of bladder neoplasms and benign prostatic hyperplasia)

• Monopolar and bipolar operating modes in cut and clot

• Bipolar resection function in saline solution

• Suitable for use in videolaparoscopic and open surgery

• Optimized to minimize damage to surrounding tissues

• Presence of optical and acoustic signaling during operation

• Maximum power output not less than 300W

• Generator activation with manual and foot control

• Control panel complete with display for setting and displaying

operation

• Mains power

• Complete with dedicated trolley for transport

• Compatible with the use of instruments suitable for laparoscopic and laparotomic surgery in various types

and dimensions

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

• Vertical blood cabinet dedicated to the storage of blood and blood components

• Floor configuration and single-body structure

• External structure in robust, non-toxic, anti-corrosion material

• Internal structure in stainless steel or equivalent stainless material with rounded edges for

ensure maximum hygiene, safety and easy sanitization

• Insulation system with high thermo-insulating power

• Nominal capacity not less than 250 liters

• Bag capacity of 450 ml not less than 150

• Single door with perimeter gasket that guarantees tightness and easy maintenance

• Glass door

• Door with lock with key or similar more advanced system

• Equipped with internal lighting;

• Equipped with at least 5 sliding and pull-out drawers and height adjustable complete with bag dividers

• Operating temperature of +4°C

• Control panel with display, from which you can clearly deduce and at the same time adjust the

Main operating parameters. At least the temperature of

exercise.

• Equipped with a system of recording/storage, monitoring, visualization and traceability of the

temperature over time with a weekly disc type system or more advanced equivalent as long as

allows immediate and continuous visualization of the temperature trend (realtime graph

always visible on display), the result is printable on paper and the monitoring of the

temperature occurs even in case of power failure

• Equipped with an acoustic / visual alarm system that allows you to promptly inform at least on

temperature anomalies, high and low, faults, door open, black-out

• Remote alarms at least through clean contact and possibly with more advanced systems

(modulo gsm, wifi, ecc.)

• Automatic defrosting system

• Equipped with 4 wheels for easy movement

• Mains power

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

Vertical biological refrigerator intended for the storage of drugs, reagents, vaccines, etc. (in order to

allow the verification of the correct destination the supplier must attach among the documentation

manual technique of use or excerpt of it from which to detect the indications of use of the product offered)

• Floor configuration and single-body structure

• External structure in robust, non-toxic, anti-corrosion material

• Internal structure in stainless steel or equivalent stainless material with rounded edges for

ensure maximum hygiene, safety and easy sanitization

• Insulation system with high thermo-insulating power

• Nominal capacity between 400 and 700 liters

• Single door with perimeter gasket that guarantees tightness and easy maintenance

• Solid door

• The door must be equipped with a lock with key or similar more advanced system

• Equipped with internal lighting

• Equipped with at least 3 height-adjustable sliding and pull-out shelves

• Equipped with automatic defrost system

• Operating temperature adjustable by the operator in a range of not less than +2 ÷ +10°C

• Control panel with display, from which you can view them clearly and at the same time

adjust the main operating parameters. At least the display must be viewable

operating temperature.

• Equipped with temperature recording, monitoring, display and traceability system in the

time with a weekly disc type system or more advanced equivalent as long as it allows the

immediate (real-time) and continuous display of the temperature trend on a digital graph,

the result is printable on paper and the temperature monitoring also takes place in

case of power failure

• Equipped with an acoustic / visual alarm system that allows you to promptly inform at least on

Temperature anomalies, high and low, faults, open door, black-out.

• Remote alarms at least through clean contact and possibly with more advanced systems

(modulo gsm, wifi, ecc.)

• Equipped with 4 swivel wheels for easy movement

• Mains power

• Compliance with applicable specific Directives and reference standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

General requirements:

High-tech two-body system dedicated to operating room lighting: main and

Ceiling-mounted satellites anchored to a single pivot point

LED lighting

Aerodynamic design to reduce turbulence due to heating of the surrounding air

Maximum manoeuvrability of the luminaires

Sterilizable handpieces

CE marking in accordance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

• Medical device for automatic reprocessing of flexible endoscopes of various brands and models

• High disinfection system through the use of peracetic acid in suitable solutions

concentrate

• Automatic dosing system of the various disinfectant agents

• Equipped with at least N. 1 washing chamber for the treatment of at least N. 1 endoscope

• Equipped with single connections for each endoscopic canal easily identifiable

• Washing and disinfection cycle consisting of at least the following phases:

leak test

washing

disinfection

rinsing

• Possibility of selecting different preset washing programs

• Execution of the endoscope leak test at least at the beginning and end of washing

• Equipped with at least N.1 complete washing program lasting no more than 40 minutes

• Self-disinfection cycle of the machine

• Intuitive and easy-to-use control panel for program access

• Display for displaying the main operating parameters (set program, duration

cycle residue, end of cycle, etc.)

• Watertight washing chamber without emission of any vapors into the environment and without the

need for dedicated suction systems

• Locking system of the washing chamber panel that prevents accidental opening of the same

during the washing cycle

• Made of materials with smooth surface resistant to the most common disinfectants used in the field

hospital

• Suitable water treatment and supply system

• Possibility of discharging residues into the common sewerage system of the hospital

• Equipped with a printer for traceability and printing of cycle documentation that contains at least

the following information: endoscope code, date, time and duration of washing

• The supply must include any compressor if the product offered requires

compressed air for its operation

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

The supply is also understood to include everything necessary for the connection of the

equipment to the existing plant; moreover, since the Sterilization Rooms in which the

devices are under construction The successful tenderer undertakes to provide all graphs and diagrams

necessary for the realization of the plant preparation useful for the correct installation of the

machines, as well as all the technical support necessary for the success of the assembly operations.

• Electric movement bed for adult patients

• Equipped with 4 sections and 3 joints

• Compact bed of maximum dimensions (including sides) not exceedable:

length of 250 cm (without the stretch function)

width of 105 cm

• Equipped with 4 wheels:

twins

Of a diameter of not less than 150 mm

antistatiche

with braking system

at least 2 swivels

• Headboard, footboard, side rails, backrest and mesh made of impact-resistant materials and

stresses, easily washable and sanitizable and resistant to corrosion

• Removable headboard and footboard, equipped with movement lock mechanism and handles

Integrated ergonomics

• Tiltable backrest, equipped with tilt indicators and movement lock mechanism

• Two side safety sides on each side for patient containment for at least 3/4 of the

The length of the network plane. The sides must be foldable and equipped with ergonomic handles

integrate

• Control panel for bed handling controls

• Safe workload of at least 200 kg

• Electrically variable height

• Equipped with audible and/or visual alarm "brake not engaged"

• Electric Trendelenburg/AntiTrendelenburg functions so that the entire support platform of the

mattress is able to reach a minimum angle of +/- 12°

• Electric movement of sections (backrest, leg) and functionality (height,

Trendelenburg/AntiTrendelenburg), via control panel

• Mechanical control to obtain the cardiopulmonary resuscitation (CPR) position

• Setup "seat / cardiology chair"

• Degree of protection against liquids at least equal to IPX4

• Complete with

protective bumpers at corners;

Battery

• Predisposition and equipped with the following accessories:

bag holder

n. 1 steel drip rod, with at least two hooks

n. 1 patient lifting rod consisting of steel rod, socket (e.g. triangle, trapezoid) and adjustable

in height (e.g. by strap) for patient lifting

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

• Luminaire in compact (or possibly modular) configuration suitable for monitoring

for adults of at least the following parameters:

ECG with detection on at least 5 sampling points

Heart rate

SpO2 with plethysmographic curve

Non-invasive blood pressure (NIBP)

Surface body temperature

• Color touch screen display of no less than 15"

• Simultaneous representation of at least 3 waveforms and all active numerical values of all

Detected parameters

• Custom configuration of tracks and parameters displayed on the display

• Intuitive and easy-to-use user interface with screens and directions in Italian

• Equipped with keys (hardware or software) immediately accessible (always in the foreground) for

Main functions (e.g. on/off, alarm silence, menu and main screen call, execution

NIBP measure)

• Equipped with software for ST tract analysis and for the recognition and classification of arrhythmias

• Acoustic and visual alarms on physiological parameters detected for anomalies or exceeding minimum values and

Maximum set, with personalized setting, for each parameter, of alarm levels

• Technical and self-diagnosis alarms (battery status, disconnected sensors, etc.)

• Storage of alarm events

• Operational messages, alarms, analysis and dialogs in Italian

• Electrically isolated mains socket for connection to the control panel via Ethernet network

• Built-in memory can store at least: up to 24 hours of graphical and tabular trends, summary

ST, 100 alarm events

• Integrated thermal printer

• Availability of future expansion with additional parameters

• Integrated wireless and/or LAN network card for predisposition to the next connection with

possible monitoring centre

• Mains and rechargeable battery power supply with autonomy of not less than 2 hours of operation at

full capacity

• Each monitor must be equipped with all accessories of use / parts applied (cables, probes, extension cords,

bracelets, sensors, electrodes, etc.) necessary for the detection of each measured parameter and for patients

adults

• Complete with dedicated trolley for transport/housing

• CE marking in compliance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

• Rotary welding process

• Suitable for welding bags for packaging sterile products

• Welding according to DIN standards

• Welding height not less than 12 mm

• Welding speed not less than 6 m/min

• Adjustable temperature at least up to a maximum of 200 ° C

• Display for reading the set and operating parameters

• Keypad for setting welding parameters

• Made of stainless steel resistant to the most common detergents used in the healthcare sector

• Integrated printer for printing information directly on the envelope during the

welding

• Mains power

• Complete with sliding plane

• Equipped with roll holder for sterilization bags with cutter

• Complies with Product Directives and Technical Standards

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the

above equipment (any connection cables, power cables, interface cables,

chargers, adapters, patient cables, cc.) and any consumables/tests for the execution of

acceptance tests.

Horizontal wall headboard beam with single module

Length of at least 150 cm

Made of anti-rust material and highly resistant to the most common detergents used in

Hospital environment

Lines that are rounded and do not allow objects to be placed on top

Physically separated compartments to group electrical utilities, lighting units and gas sockets

Medical

LED lighting for each bed that can be operated with screen-printed switch/keyboard/panel

present on the beam and optionally with wire control divided into:

o Light patient area for medical examination

o Diffused light, not directed to the patient, to illuminate the room

o Night diffused light

o Reading light

Minimum equipment:

o N. 3 universal electrical sockets BIPASSO + SCHUKO type 2P+T 10/16 A

o N. 3 universal electrical sockets BIPASSO type 2P+T 10/16 A

o N.2 medical gas sockets UNI 9507 (Vacuum, Oxygen)

o N.1 press USB

o N.1 remote control for emergency call

Integrated normalized bar to allow you to hook any equipment

electromedical (such as infusion pumps, monitors, bubblers, etc.)

CE marking in accordance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

Made of shockproof material, compact, shiny and smooth enough to eliminate all sharp parts and

Pointed

Approximate dimensions of approximately 180 cm long and 150 cm wide

Ergonomic shape that allows the expectant mother to move freely, stretch her legs,

kneeling, on all fours, giving birth and, to the midwife, to attend the birth in conditions

ergonomically appropriate

Large door to allow the patient to enter comfortably without risk of

Falls

Pair of handles for support

Thermostatic tank edge mixer and diverter with conversion to shower

Antibacterial and anti-legionella filtering system of incoming water

Automatic filling system

Digital temperature indicator

System for constant temperature maintenance

Suction and maceration system of foreign bodies

Double step for accessibility

Suspended rope system (hook, vine and carabiner)

Fetal monitor for cardiotocographic monitoring equipped with:

o Waterproof toco and cardio probes, wireless with wide range, powered by

battery, can be used for tank monitoring

o Receiving station for charging probes powered by the mains

CE marking in accordance with Directive 93/42/EEC and subsequent amendments. or the new MDR

2017/745 and subsequent amendments. and all relevant technical reference product standards

These technical specifications govern the supply of an autoclave system consisting of:

N.1 steam autoclave of 6 UdS

N.1 steam autoclave of 2 Uds

N.1 water treatment system serving the above autoclaves

Supply of specific equipment for the technical furnishing of operating blocks.

Video processor and camera, Light source, Monitor, Recording and archiving system, Trolley, CO2 insufflator, Irrigator/aspirator, Rigid optics.

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the above equipment (any connection cables, power cables, interface cables, battery chargers, adapters, patient cables, cc.) and any consumables / tests for the execution of the acceptance tests. The supply is also understood to include everything necessary for the interfacing of the components with each other.

Generator, X-ray source (with reference to standards: IEC 60613, IEC 60336 and CEI 60601), Image formation and management system, Multidirectional C-arc monoplanar stand, Mobile c-arc user interface, DICOM standard and connectivity ports, Image examination and processing techniques, Mobile visualization station. The Supply is complete with all the accessories and modules necessary for the correct and complete use of the above equipment (any connection cables, power cables, interface cables, battery chargers, adapters, patient cables, cc.) and any consumables / tests for the execution of the acceptance tests. The supply is also understood to include everything necessary for the interfacing of the components with each other.

Wall cabinet system with ceiling installation

Single column head anchored on supporting structure

Suitable for both surgery and anesthesia

Edge-free and made of disinfection-resistant construction material and easily

sanitized with the most common detergents used in hospitals

Column length not less than 100 cm

High extension of the arm(s)

Degree of rotation of the joints not less than 300°

Vertical travel not less than 600 mm

Pneumatic or higher braking system

Locking system to prevent accidental movements

Handles and/or push-button panel with controls for movement

Total payload capacity not less than 150 Kg

Tested complete with at least the following elements:

o n.2 Oxygen socket with UNI connection

o n.1 medical air socket with UNI connection

o n.1 high pressure compressed air intake

o n.2 socket Empty UNI connection

o n.1 anesthetic gas evacuation socket type UNI

o n.8 combined electrical sockets (10A/16A/schuko) individually protected

or n.2 data sockets type RJ45

o n.1 height-adjustable shelf

or n.1 shelf with drawer

Column, patient table, trolley, accessories.

The Supply is complete with all the accessories and modules necessary for the correct and complete use of the above equipment (any connection cables, power cables, interface cables, chargers, adapters, patient cables, etc.) and any consumables / tests for the execution of the

acceptance tests. The supply is also understood to include everything necessary for the interfacing of the components with each other.

The system must be suitable for minimally invasive robot-assisted surgeries, in

video-assisted endoscopic surgery managing to maximize anatomical access and ensuring a

3D-HD vision.

The proposed system must be complete with all the components, main and accessories, necessary to

perform surgical interventions related to the following clinical specialties (indicative and non-exhaustive):

UROLOGY (prostatectomy, partial and radical nephrectomy, pyeloplasty, etc.)

GENERAL AND ONCOLOGICAL SURGERY (colorectal surgery, hepato-biliopancreatic surgery,

bariatric surgery, etc.)

GYNECOLOGY (hysterectomy, myomectomy, endometrial resection, etc.)

OTOLARYNGOLOGY (oropharyngological tumors, thyroidectomy, etc.)

GENERAL CHARACTERISTICS Defibrillator with advanced functions for monitoring physiological parameters Suitable for use on ambulances and rescue operations Can be used on adults and children Operating temperature: minimum range 0-40°C Small size and weight, easily transportable and sanitizable Degree of protection from external agents at least IP55 Powered by high-capacity rechargeable battery Equipped with thermal printer preferably integrated for ECG printing, self-test defibrillator, etc.