LYMPHEDEMA SYSTEM BUYER GUIDE

How to source a lymphedema compression system.

Written by Ming Cheng, Product & Export Manager, HuanYu Health.

Review the equipment, garment and documentation questions that matter when evaluating a sequential pneumatic compression system.

Last checked: September 10, 2026. Source basis: HuanYu Health product catalogue and current model documentation. Verify specifications with HuanYu Health before ordering.

24D portable sequential pneumatic compression system for lymphedema care

What is a lymphedema compression system?

A lymphedema compression system combines a pneumatic pump with a multi-chamber garment to deliver sequential compression. Equipment buyers should verify pressure settings, chamber sequence, garment coverage, home-use suitability and approved documentation.

Key evaluation criteria

Pressure and sequence

Compare the default pressure, adjustment method, chamber sequence and cycle timing against the approved use case.

Garment fit and coverage

Garment construction, size range, limb coverage and tubing layout affect compatibility and daily setup. Confirm every accessory by model.

Home-care workflow

For portable use, review charging time, battery operation, device weight, controls, cleaning instructions and user training materials.

The 24D values below are catalogue references, not clinical recommendations. Confirm the current configuration and documents with HuanYu Health before quotation.

24D portable system reference

The 24D portfolio reference includes a 50 mmHg default pressure, approximately 75 × 125 × 33 mm dimensions and 0.32 kg weight. These values are selected catalogue references and must be confirmed for the final configuration.

Review the 24D specification summary →

Frequently asked questions

Is a lymphedema compression pump suitable for home use?

Suitability depends on the approved intended use, prescription or clinical guidance, user training and the specific model configuration.

Which garments work with the 24D system?

Garment type, size, chamber layout and connector compatibility must be confirmed against the current product documentation.

What documents should importers request?

Request the current catalogue, instructions for use, model specifications, available regulatory documents and packaging information for the destination market.