Efor Ekg Sistemi Custo Med

İlan No: #00113940
Fiyat Sorunuz
Kategori: Fizik Tedavi
Marka: Custo Med
Model Yılı: 2019
Ürün Tipi: Satılık
Ürün Durumu: Sıfır ( Yeni )
Menşei: Almanya
Teslim Durumu: 7 Gün
Konum: Maltepe / İstanbul / Türkiye
Kısa Detay: Yıl Garantili
Satış Detayı: Vade Olur, Leasing'e Uygun

Efor Ekg Sistemi Custo Med

 

Technical data of custo cardio 100/110/130
Frequency response 0.05 – 500 Hz
Accuracy < 1.5%
Time constant 3.2 sec
Sampling rate 1.0ms / 1000 Hz for extremities and thoracic wall
0.25ms/ 4000 Hz for pacemaker
A/D converter 24 bit
Input impedance > 50 MΩ
Amplitude quantification 0.3 μV/bit
CMRR > 70 dB
Impedance measurement *) At all electrode leads (not N) with automatic quality indication
Defibrillation protection Electrical strength 5000 V
Recovery time after defibrillation < 10s
Voltage supply USB devices USB cable
BT devices Rechargeable lithium-ion battery
Energy consumption Max. 2.5 watt during recording
IT connection *) USB (cable length 2.50 m)
Bluetooth range Up to 80 m, depending on ambient conditions
Software, additional functions Power filter, muscle filter,
(custo diagnostic) AD filter (Anti-drift), pacemaker recognition
Operating conditions Temperature +10°C ... +40°C
Air humidity 30 ... 80% rH
Air pressure 700 ... 1060 hPa
Transport and storage Temperature -20°C ... +45°C
conditions Air humidity 30 ... 80% rH
Air pressure 700 ... 1060 hPa
Size custo cardio 100/110 approx. 160 * 85 * 25 mm (L * W * H)
custo cardio 130 approx. 160 * 78 * 32 mm (L * W * H)
Weight custo cardio 100/110 approx. 300 g
custo cardio 130 approx. 430 g
Patientleads custo cardio 100 ERG approx. 600 – 700 mm (extremities)
approx. 500 – 650 mm (chest)
custo cardio 100/110 approx. 1050 mm (extremities)
approx. 700 mm (chest)
custo cardio 130 15-pin ECG input connector
(D-Sub screw connection or Siemens plug)
Classification Safety class II (custo cardio 100/110/130 USB)
Safety class III (custo cardio 100/110 Bluetooth)
Class IIa
Type BF defibrillation protected (not intracardiac)
DIN EN 60601-1
DIN EN 60601-2-25
DIN EN 60601-2-51
 
TREADMİLL
EC manufacturer's declaration of conformity
For the following designated product
Product: ergo_run
Model: ergo_run medical8
We hereby declare that the aforementioned product complies with the following prescriptions:
EC-directive 93/42EEC of the council of June 14, 1993 about medical products
The following standards and prescriptive provisions were used to evaluate the product:
Standard description Issue
EN 1041 Information supplied by the manufacturer 1998
with medical devices
EN 60601-1 + A1 + A2 Medical electrical equiqment Part 1 - 1994
General requirements for safety
EN 60601-1-2 Medical eletrical equipment Part 1 - 2001
General requirements for safety
2. additional form : electromagnetic compatibility -
requirements and tests
The quality assurance system of daum electronic gmbh is certified by the DQS GmbH according to the
representation models ISO 13485:2003 and according to 93/42EEC annexe II item 3, (CE 0297).
EC manufacturer's declaration of conformity
For the following designated product
Product: ergo_run
Model: ergo_run medical8
We hereby declare that the aforementioned product complies with the following prescriptions:
EC-directive 93/42EEC of the council of June 14, 1993 about medical products
The following standards and prescriptive provisions were used to evaluate the product:
Standard description Issue
EN 1041 Information supplied by the manufacturer 1998
with medical devices
EN 60601-1 + A1 + A2 Medical electrical equiqment Part 1 - 1994
General requirements for safety
EN 60601-1-2 Medical eletrical equipment Part 1 - 2001
General requirements for safety
2. additional form : electromagnetic compatibility -
requirements and tests
The quality assurance system of daum electronic gmbh is certified by the DQS GmbH according to the
representation models ISO 13485:2003 and according to 93/42EEC annexe II item 3, (CE 0297).

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