Resources & downloads

Accel‑Heal® is certified as a Class IIa medical device under the Medical Device Directive 93/42/EEC.

Accel‑Heal® carries the CE mark having been approved by Notified Body 1639. Accel‑Heal® is manufactured in accordance with the requirements of ISO 13485:2016 for the design and manufacture of medical devices.

Accel-Heal Brochures

Case Studies Brochure (PDF)

Accel‑Heal Overview (PDF)

Accel‑Heal Application Guide (PDF)

Accel‑Heal Product Monograph (PDF)

Accel‑Heal Instructions for use (PDF)

Accel‑Heal Instructions for use - en Francais (PDF)

Accel‑Heal Patient Leaflet (PDF)

Accel-Heal Solo Brochures

Accel-Heal Solo Application Guide (PDF)

Accel-Heal Solo Sales Aid (PDF)

Accel-Heal Solo Patient Information Leaflet (PDF)

Accel‑Heal Solo Instructions for use (PDF)

Accel‑Heal Solo Instructions for use - en Francais (PDF)

Videos

Accel‑Heal Overview

Accel‑Heal with Compression Bandaging

Accel‑Heal without Compression Bandaging

Accel-Heal Device Change

Accel-Heal Patient Experience

How to use Accel-Heal with Compression Bandages

Quality & Certification

ISO 13485:2016 (PDF)

MDD 93/42/EEC Certificate (PDF)

Declaration of Conformity (PDF)

Conference & Professional Education Presentations

Posnett EWMA 2020: Cost-effectiveness of a single- use, portable electrical stimulation device in the management of venous leg ulcers (PDF)

Published Reviews

Electrical stimulation for pain reduction in hard-to-heal wound healing (PDF)

How to order Accel-Heal and Accel-Heal Solo