Seca CT8000i ECG Machine with 10-Lead ECG Leads, New Clearance Stock

Seca CT8000i ECG Machine with 10-Lead Leads Included

The Seca CT8000i is a clinical ECG machine supplied by SECA, listed here as new clearance stock and including a set of 10-lead ECG leads in the box. It is intended for use in clinical settings where a complete, ready-to-connect electrocardiograph is required.

What is included

What is not included

Checked before dispatch

This unit is listed as new clearance stock. Before dispatch, Elarix Medical carries out the following in-house workshop checks:

• Visual inspection for cosmetic condition and completeness
• Contents checked against stated inclusions
• Powered on and basic function confirmed where applicable

These are in-house workshop checks only. Damaged or non-working items are not dispatched. A full engineer service and calibration is not included unless this listing states the unit has been serviced. Commissioning, verification, planned maintenance and periodic electrical safety testing remain with the operating organisation.

Why this matters

A 12-lead ECG remains a standard diagnostic investigation in cardiology, acute medicine and general practice. Having the ECG leads supplied in the box means the unit can be connected immediately without sourcing compatible cables separately, which is a practical advantage at point of purchase.

SECA is an established manufacturer of clinical diagnostic equipment. The CT8000i is designed for professional clinical use. The product code held in this store's record is 9740400220.

Consumables and compatibility

ECG electrodes are single-use and must be sourced separately. Ensure any electrodes ordered are compatible with the lead connectors supplied. Check with your clinical supplies team or the SECA distributor for compatible electrode types. Thermal paper, if required by this model, is also a consumable and is sold separately.

Regulatory note

This device is classified as active medical equipment. Commissioning, periodic electrical safety testing and planned maintenance are the responsibility of the operating organisation and should be carried out in accordance with local clinical engineering protocols and relevant regulations including PUWER.

Information on this page is provided for guidance and does not replace advice from a qualified clinician. Always read the manufacturer's instructions before use, and check that a device is suitable for the patient and the prescribed therapy.