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Temedica GmbH

Germany Last updated 21 Oct 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • Brisa Ref Brisa

    Class IIa EUDAMED Active

About

Empowering pharma brands with AI-powered solutions, real-world insights, and fully automated, compliant omnichannel engagement — from launch acceleration to long-term persistence.

From the manufacturer's own website. Source

What Temedica GmbH makes

Temedica GmbH manufactures the Brisa system, an automated platform designed for omnichannel engagement in pharmaceutical marketing and patient persistence programs. The solution integrates AI-driven analytics and real-world data to support targeted outreach and compliance with regulatory requirements.

The Brisa system is classified as a Class IIa medical device and is registered in the EU’s eudamed database. Temedica GmbH is based in Germany.

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

Frequently asked questions

How many devices does Temedica GmbH have in the registry?

The registry currently lists 1 device for Temedica GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Temedica GmbH's devices?

Among its 1 most recently registered device, Temedica GmbH has devices listed in EUDAMED (1 device).

What risk classes do Temedica GmbH's devices fall under?

Among its 1 most recently registered device, the classes recorded for Temedica GmbH's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Temedica GmbH in the registry?

The most recently registered devices listed for Temedica GmbH include Brisa.

Generated automatically from registry data and not verified by a human reviewer.

Information

Address
21, Erika-Mann-Straße, München, Germany
PRRC contact
Gloria Seibert
EUDAMED SRN
DE-MF-000006165