Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

ToLife Technologies Pty. Ltd.

Australia·AU-MF-000036510

Last updated September 18, 2026

About

The V-Comb is a revolutionary device that incorporates both a combing & vacuum function to effectively eliminate traces of head lice.

From the manufacturer's own website. Source

What ToLife Technologies Pty. Ltd. makes

ToLife Technologies manufactures manual head lice removal devices, including the V-Comb A1 and V-Comb Edge. These products combine a comb with a vacuum function to physically remove lice and nits from hair during use.

The company’s devices are classified as Class I under EU regulations and are listed in the EU’s eudamed database. The manufacturer is based in Australia.

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 ToLife Technologies Pty. Ltd. manufacture?

ToLife Technologies Pty. Ltd. specializes in manual head lice removal devices. Their products, such as the V-Comb A1 and V-Comb Edge, combine a comb with a vacuum function to physically remove lice and nits from hair during use. These devices are designed for non-invasive, at-home treatment of head lice infestations.

Where is ToLife Technologies Pty. Ltd. based?

ToLife Technologies Pty. Ltd. is based in Australia. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the provided information.

Are ToLife Technologies’ devices listed in any regulatory registries?

Yes, ToLife Technologies’ devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. This listing is relevant for transparency and traceability of devices marketed in the EU, though it does not imply regulatory approval for the company or its products.

How are ToLife Technologies’ devices classified under EU regulations?

ToLife Technologies’ devices, such as the V-Comb A1 and V-Comb Edge, are classified as Class I under EU medical device regulations. This classification is typically assigned to low-risk devices that pose minimal risk to patients, such as manual removal tools for head lice. The classification determines the regulatory requirements for their market placement.

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

Information

Country
Australia
Address
53, Banksia Road, Welshpool, Western Australia, Australia
LinkedIn
—
Facebook
—
Phone
+61 8 9350 5688
PRRC Contact
Joseph Carpio
EUDAMED SRN
AU-MF-000036510
FDA FEI Number
—
DUNS Number
—

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
V-Comb A1 TTA101
EUDAMED
Class IActive
V-Comb Edge TTE01
EUDAMED
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.