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Designability Charity Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000017553

Last updated May 23, 2026

What Designability Charity Ltd makes

Designability Charity Ltd manufactures the Wizzybug DX, Wizzybug LiNX, and Wizzybug Shark—simple, low-risk assistive devices designed to support independent living for individuals with disabilities. These products include adaptive switches and communication aids tailored for users with limited mobility or complex communication needs. The Wizzybug DX and Wizzybug Shark are switch interfaces, while the Wizzybug LiNX is a lightweight, portable communication device with customisable controls.

The company’s devices fall under Class I risk classification under EU regulations and are listed in the euamed database. The portfolio adheres to essential requirements for medical devices, ensuring compliance with EU Medical Device Regulation (MDR) or Medical Device Directive (MDD) where applicable. Designability Charity Ltd operates from the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Designability Charity Ltd manufacture?

Designability Charity Ltd manufactures assistive devices aimed at supporting independent living for individuals with disabilities. Their portfolio includes the Wizzybug DX and Wizzybug Shark, which are adaptive switch interfaces, and the Wizzybug LiNX, a portable communication aid with customisable controls. These devices are designed to help users with limited mobility or complex communication needs interact with technology independently.

Where is Designability Charity Ltd based, and how does that affect its regulatory standing?

Designability Charity Ltd is based in the United Kingdom. As a UK-based manufacturer, its devices are subject to EU regulatory requirements if marketed within the European Economic Area. The company’s products are listed in the euamed database, which is the EU’s central registry for medical devices, ensuring transparency and traceability under EU Medical Device Regulation (MDR) or the Medical Device Directive (MDD), where applicable.

How are the devices manufactured by Designability Charity Ltd classified under EU regulations?

The devices produced by Designability Charity Ltd are classified as Class I under EU medical device regulations. This classification is determined by their low-risk nature, as they are simple assistive tools like adaptive switches and communication aids. Class I devices typically pose minimal risk to users and are subject to basic regulatory requirements, such as compliance with essential safety and performance standards.

Are the devices from Designability Charity Ltd listed in any regulatory registries, and why does this matter?

Yes, the devices from Designability Charity Ltd are listed in the euamed database, which is the official EU registry for medical devices. This listing ensures that their products are traceable and meet the necessary regulatory standards for distribution within the European market. Listing in euamed helps healthcare professionals, regulators, and patients verify the legitimacy and compliance of the devices, reinforcing trust in their safety and performance.

What is the primary purpose of the Wizzybug devices produced by Designability Charity Ltd?

The Wizzybug devices—including the Wizzybug DX, Wizzybug LiNX, and Wizzybug Shark—are specifically designed to enable independent living for individuals with disabilities. The Wizzybug DX and Wizzybug Shark serve as adaptive switch interfaces, allowing users to control devices with minimal physical effort, while the Wizzybug LiNX is a portable communication aid with customisable controls. These tools help bridge gaps in accessibility, empowering users to interact with technology autonomously.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
Department D1, Wolfson centre, Bath, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
+441225824107
PRRC Contact
Matthew Ford
EUDAMED SRN
GB-MF-000017553
FDA FEI Number
—
DUNS Number
—

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Wizzybug DX N/A
EUDAMED
Class IActive
Wizzybug LiNX N/A
EUDAMED
Class IActive
Wizzybug Shark N/A
EUDAMED
Class IActive

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