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2011 - Nihon Kohden - Cardiofax ECG-1350K - Electrocardiograph
- Aktuelles Gebot
- Status
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Spezifikationen zum Los
- Menge
- 1
- Differenzbesteuerung
- Nein
- Marke
- Nihon Kohden
- Typ
- Cardiofax ECG-1350K
- Baujahr
- 2011
- Lieferbedingungen
- Verladung auf LKW
Beschreibung
Nihon Kohden Cardiofax ECG-1350K (2011)
is a digital electrocardiograph designed for recording and analyzing the electrical activity of the heart. Manufactured by Nihon Kohden, Japan, this device is intended for use in hospitals, clinics, and other healthcare facilities for routine cardiac examinations.
The ECG-1350K features a display for viewing ECG waveforms and patient information, as well as an integrated thermal printer for producing printed ECG reports. It supports electrocardiographic recordings and provides measurement and analysis functions to assist healthcare professionals in evaluating cardiac activity. Depending on the installed configuration, the device can offer automatic ECG interpretation and options for storing or transferring examination data.
Designed for practical use in medical environments, the Cardiofax ECG-1350K provides a convenient solution for routine electrocardiographic examinations. Its compact design allows it to be placed on a suitable medical trolley for easier mobility and positioning within the examination room.
Although manufactured in 2011, the device may remain suitable for clinical use if it is in good working condition, properly maintained, and verified to meet applicable medical electrical safety and performance requirements.
After the auction has ended, the buyer must contact the seller by email to arrange shipping and delivery of the package.
Collection (pick-up) must be arranged by the buyer. Functional testing and verification are not available on-site during collection.
is a digital electrocardiograph designed for recording and analyzing the electrical activity of the heart. Manufactured by Nihon Kohden, Japan, this device is intended for use in hospitals, clinics, and other healthcare facilities for routine cardiac examinations.
The ECG-1350K features a display for viewing ECG waveforms and patient information, as well as an integrated thermal printer for producing printed ECG reports. It supports electrocardiographic recordings and provides measurement and analysis functions to assist healthcare professionals in evaluating cardiac activity. Depending on the installed configuration, the device can offer automatic ECG interpretation and options for storing or transferring examination data.
Designed for practical use in medical environments, the Cardiofax ECG-1350K provides a convenient solution for routine electrocardiographic examinations. Its compact design allows it to be placed on a suitable medical trolley for easier mobility and positioning within the examination room.
Although manufactured in 2011, the device may remain suitable for clinical use if it is in good working condition, properly maintained, and verified to meet applicable medical electrical safety and performance requirements.
After the auction has ended, the buyer must contact the seller by email to arrange shipping and delivery of the package.
Collection (pick-up) must be arranged by the buyer. Functional testing and verification are not available on-site during collection.
Anmerkungen
The equipment is offered as used medical equipment in its existing condition.
Information regarding functionality, accessories, and overall condition is provided to the best of our knowledge based on the available information and visual inspection. Unless explicitly stated otherwise, the technical and functional condition has not been verified.
The calibration status, service history, electrical safety status, and full operational functionality have not been confirmed.
The equipment is offered on an “AS IS” basis, without any express or implied warranty or guarantee, to the extent permitted by applicable law.
The sale includes only the equipment and accessories explicitly shown in the listing photographs or specified in the description. The presence of measurement modules, patient cables, sensors, and other accessories should not be assumed unless expressly confirmed.
Pursuant to the German Medical Devices Act (MPG) and the applicable EU directives, the item described is sold as DEFECTIVE (“used for hobbyists/repair purposes”) or as a “spare parts donor”, without any warranty or guarantee, even though the device is functional. Any liability for defects arising after delivery is excluded. The buyer is expressly advised that, when putting the device into operation, they must comply with the applicable provisions of the Medical Devices Act (MPG) and the German Medical Devices Operator Ordinance (MPBetreibV). Where required, the device must also undergo an appropriate safety-related inspection (STK). The buyer is solely responsible for ensuring compliance with these requirements.
Information regarding functionality, accessories, and overall condition is provided to the best of our knowledge based on the available information and visual inspection. Unless explicitly stated otherwise, the technical and functional condition has not been verified.
The calibration status, service history, electrical safety status, and full operational functionality have not been confirmed.
The equipment is offered on an “AS IS” basis, without any express or implied warranty or guarantee, to the extent permitted by applicable law.
The sale includes only the equipment and accessories explicitly shown in the listing photographs or specified in the description. The presence of measurement modules, patient cables, sensors, and other accessories should not be assumed unless expressly confirmed.
Pursuant to the German Medical Devices Act (MPG) and the applicable EU directives, the item described is sold as DEFECTIVE (“used for hobbyists/repair purposes”) or as a “spare parts donor”, without any warranty or guarantee, even though the device is functional. Any liability for defects arising after delivery is excluded. The buyer is expressly advised that, when putting the device into operation, they must comply with the applicable provisions of the Medical Devices Act (MPG) and the German Medical Devices Operator Ordinance (MPBetreibV). Where required, the device must also undergo an appropriate safety-related inspection (STK). The buyer is solely responsible for ensuring compliance with these requirements.
Weitere Details
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