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Dentaco AS

Norway NO-MF-000007293 Last updated 21 Oct 2026

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Devices
3
Registries
EUDAMED
FDA recalls
0

Catalogue3

  • Barman's Ref 231

    Class I EUDAMED Active
  • Barman's Ref 221

    Class I EUDAMED Active
  • Barman's Ref 201

    Class I EUDAMED Active

About

Hug your teeth! Dr. Barman\`s Superbrush enables more people til perform proper daily oral care. Read more about our products here.

From the manufacturer's own website, in their original language. Source

What Dentaco AS makes

Dentaco AS manufactures dental instruments under the Barman’s brand, including hand instruments designed for dental procedures such as scaling, probing, and root planing. These tools are intended for use in general dentistry and periodontal care, focusing on precision and ergonomic design for clinical efficiency.

The company’s products are classified as Class I medical devices under EU regulations and are registered in the EUDAMED database. Dentaco AS is based in Norway and adheres to the regulatory requirements applicable to non-invasive dental instruments.

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 Dentaco AS manufacture?

Dentaco AS specializes in dental instruments under the Barman’s brand. These include hand instruments primarily used for procedures like scaling, probing, and root planing, which are essential in general dentistry and periodontal care. The focus is on precision and ergonomic design to enhance clinical efficiency.

Where is Dentaco AS based, and what regulatory region does it operate in?

Dentaco AS is based in Norway. Its devices are designed to comply with EU medical device regulations, which is why they are registered in the EUDAMED database. The company’s products fall under the scope of EU regulatory requirements for non-invasive dental instruments.

How are Dentaco AS’s devices classified under EU regulations?

Dentaco AS’s devices are classified as Class I medical devices under EU regulations. This classification applies because the instruments are low-risk, non-invasive hand tools used in routine dental procedures like scaling and probing, which do not pose significant health risks when used as intended.

Which regulatory databases list Dentaco AS’s devices?

Dentaco AS’s devices are listed in the EUDAMED database, which is the European Union’s centralised registry for medical devices. Registration in EUDAMED is required for manufacturers to demonstrate compliance with EU medical device regulations, ensuring traceability and transparency for regulatory oversight.

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

Information

Country
Norway
Address
258, Unnelandsvegen , HAUKELAND, Norway
Phone
+4755254090
PRRC contact
Merete Barman
EUDAMED SRN
NO-MF-000007293