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ELECTROCARDIOGRAPH (Schiller AT-1), portable, 3 channels+ACC

https://unicat.msf.org/cat/product/12756
NST EEMDECGE1--

Discontinued Article

Former Code(s): EHOEECGR1P-
CE marking: declaration that the product meets EU standards for health, safety, and environmental protection. The CE marking indicates that the product may be sold freely in any part of the European Economic Area, regardless of its country of origin.
IIa
In Europe, medical material that fulfills the definition of a medical device according to the MDR (Medical Device Regulation) is classified into 4 classes
P
The order of this product needs to be justified and is only acceptable under certain conditions.
OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)

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ELECTROCARDIOGRAPH, portable, Schiller AT-1

Stopped in 2017 because no longer produced and replaced by the new model Schiller AT-1 G2 EEMDECGE4-- (see“replaced by” at bottom of the page).

Definition

Apparatus allowing to record and to report on a support the cardiac activity . It enables the diagnosis of cardio-vascular diseases.

The Shiller AT-1 ECG is no longer manufactured, it is replaced by the Shiller AT-1 G2

Specifications

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Quality standards

EN 60601-2-25, 2015, Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs

Technical specifications

  • Sensitivity: 5 /10 / 20 mm/mV, automatic or manual setting
  • Automatic or manual recording mode
  • Leads: Standard / Cabrera
  • Automatic program of the measurements: presentation on 3 channels of all 12 simultaneously acquired standard leads
  • ECG amplifier: simultaneous acquisition, synchronised with 9 active electrode signs (= 12 standard leads)
  • Myogram (muscle tremor) filter
  • Patient input circuitry: fully floating and isolated, defibrillation protected
  • Wastage of current at patient <5 μA
  • Built-in thermal printer
  • Power supply:100-115 / 220-240 VAC , 50/60 Hz
  • Power consumption: max. 28 VA
  • Built-in rechargeable 12 V battery:
    • charging time: 3 hours to 60 % capacity, less than 7 hours to 90% capacity
    • a fully charged battery allows 2 hours of normal use
  • Dimensions: 290 x 210 x 69 mm
  • Weight: 2.9 kg

Packaging & Labelling

Unit packaging

(Cf Introduction: Packaging and labelling)

Supplied with the Article

  • 10-lead patient cable with banana plugs
  • Power cable
  • Electrode gel tube (50 ml)
  • Precordial electrodes
  • Limbs electrodes
  • Ream of thermo-reactive, z-folded recording paper
  • Instructions leaflet
  • Carrying bag

Instructions for use

The manual mode allows the printing in real time of 3 selected leads on the built-in thermal printer.

Before or during the recording, it is possible to select the following parameters:

  • Group of leads
  • Printing speed
  • Sensistivity
  • Myogram filter

In the automatic mode, a complete ECG with 12 leads is printed in one of the 2 pre-defined report formats at a sensitivity which can be selected. These formats can be
chosen by the user according the specific needs.

When pushing on the AUTO GAIN button before the recording in automatic mode, the apparatus detects the very important amplitude peaks and adjusts the sensitivity
of the extremity and /or precordial leads to reduce the overwriting of the graphs.

Precautions for Use

  • When used or stored, the apparatus must be protected from humidity, dust, direct sunlight or any other heat source
    • working temperature: 10° to 40°C
    • storage temperature: -10° to 50°C
  • Avoid contact with steam or liquids containing acids which could cause irreversible damages to this apparatus
  • Do not install the apparatus in the neighbourhood of radiography units
  • Contact your biomedical officer in order to see the need to protect the apparatus with a double conversion UPS (see related articles below).

MSF requirements

Lightweight, compact and autonomous apparatus

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