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.

Clinician 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 Patient Leaflet (PDF)

Videos

Accel‑Heal Overview

Accel‑Heal with Compression Bandaging

Accel‑Heal without Compression Bandaging

Accel-Heal Device Change

Accel-Heal Patient Experience

Made Easy Videos

Electrical Stimulation

It’s mode of action and impact on pain and healing

Presented by Dr Robin Martin PhD

Improving pain management review your practice

Case study

Presented by Tracey Dermody MSc

The Impact of pain for patients with venous ulcers

The role of electrical stimulation

Presented by Dr Leanne Atkin PhD, MHSc, RGN

Quality & Certification

ISO 13485:2016 (PDF)

MDD 93/42/EEC Certificate (PDF)

Declaration of Conformity (PDF)

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