Non invasive Products

  • Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM
  • Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM
  • Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM
Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TMPortable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TMPortable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM

Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM

  • Brand / Model: PSK P-ECP/TM
  • Dimensions: 790 × 520 × 1010 mm
  • Net Weight: 133 kg
  • Power Supply: 220–240 V
  • INQUIRY

Portable Enhanced External Counterpulsation (EECP) System – PSK P-ECP/TM

Product Overview

The PSK P-ECP/TM Portable Enhanced External Counterpulsation (EECP) System is a non-invasive cardiovascular therapy device designed for external counterpulsation treatment in clinical environments.

The system uses ECG-synchronized pneumatic compression technology to coordinate the inflation and deflation of cuffs positioned around the patient's lower limbs.

Featuring a mobile, wheeled configuration, the P-ECP/TM model can be moved between treatment rooms and used alongside compatible treatment tables, hospital beds or reclining chairs.

It is designed for healthcare facilities evaluating non-invasive cardiovascular therapy equipment.

Technical Specifications

Parameter Specification
Product Name Portable Enhanced External Counterpulsation System
Brand PSK
Model P-ECP/TM
Product Type Portable / Mobile EECP System
Technology ECG-Synchronized Pneumatic Counterpulsation
Dimensions (L × W × H) 790 × 520 × 1010 mm
Net Weight 133 kg
Power Supply 220–240 V
Deflation Mechanism Vacuum-Assisted Pneumatic System
Equipment Configuration Mobile Unit
Treatment Pressure Range To Be Confirmed
Rated Power To Be Confirmed
Packaging Dimensions To Be Confirmed
Regulatory Certifications To Be Verified

Working Principle

Enhanced External Counterpulsation (EECP) is a non-invasive cardiovascular therapy technique involving the controlled inflation and deflation of pneumatic cuffs around the lower extremities.

The treatment process is synchronized with the patient's cardiac cycle through ECG monitoring.

The general operating principle includes:

1. Patient Positioning

The patient lies on a suitable treatment table, hospital bed or reclining chair.

2. ECG Monitoring

ECG electrodes are used to monitor the cardiac rhythm and provide synchronization signals for the counterpulsation system.

3. Pneumatic Cuff Placement

Pneumatic cuffs are positioned around the calves, thighs and buttocks.

4. Sequential Compression

The system controls cuff inflation and deflation in synchronization with the cardiac cycle.

5. Vacuum-Assisted Deflation

A vacuum-assisted pneumatic system supports rapid cuff deflation as part of the counterpulsation process.

The device must be operated by trained healthcare professionals in accordance with the manufacturer's current instructions for use.

Key Product Features

1. Portable and Mobile Configuration

The P-ECP/TM model features a wheeled design, allowing equipment movement between treatment areas within a healthcare facility.

2. ECG-Synchronized Counterpulsation

The system uses cardiac rhythm information to coordinate pneumatic cuff inflation and deflation.

3. Computer-Controlled Operation

The device incorporates computer-based control technology and a software-controlled operating system.

4. Vacuum-Assisted Pneumatic System

The pneumatic system includes vacuum pump assistance for cuff deflation.

5. Noise and Heat Management

The manufacturer's existing product description states that the system is designed to minimize operating noise and heat buildup.

6. Patient Comfort-Oriented Design

The equipment is designed with patient comfort and clinical usability in mind.

Intended Clinical Environment

The mobile EECP system may be evaluated for use in:

  • Cardiovascular treatment departments

  • Hospitals and specialized cardiovascular clinics

  • Outpatient cardiovascular therapy facilities

  • Cardiac rehabilitation facilities

  • Medical centers providing physician-supervised EECP treatment

Specific indications, patient eligibility, contraindications and treatment protocols must follow the manufacturer's approved instructions for use and applicable local regulatory requirements.

Safety and Regulatory Considerations

Enhanced external counterpulsation treatment requires professional patient assessment, appropriate monitoring and trained clinical supervision.

Before procurement or clinical deployment, buyers should confirm:

  • Manufacturer's approved intended use and indications

  • ECG and blood pressure monitoring configuration

  • Cuff pressure operating range

  • Treatment safety controls

  • Applicable contraindications

  • Electrical safety documentation

  • Available product registration and certification

  • User manual and service documentation

  • Installation, training and maintenance requirements

Regulatory approval and clinical suitability vary by market and device configuration.

International Procurement and Supply Support

Zhanmed Limited assists international distributors, hospitals and medical equipment procurement companies with China-based medical device sourcing and supplier coordination.

Our services include:

  • Product and manufacturer communication

  • Technical specification coordination

  • Commercial quotation inquiries

  • Available certificate and documentation requests

  • Export logistics coordination

  • Distributor and project procurement support

Availability, warranty, after-sales service and supply conditions are subject to manufacturer confirmation.

Request a Quotation

For technical specifications, available configurations, pricing, product documentation and international procurement inquiries, please contact:

ZHANMED LIMITED

Contact: Daniel Zhan

Email: zhanmc@zhanmed.com

WhatsApp: +86 15215105391

For professional healthcare and medical equipment procurement. Clinical use must comply with the manufacturer's approved instructions and applicable medical device regulations.