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AI Medical Technology AIM AB

Sweden SE-MF-000030500 Last updated 21 Oct 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • Dermalyser Ref Version 1.0.0

    Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G15 116811 0003 Issued

    Quality management system EU MDR

    Issued
    18 Sep 2026
    Expires
    6 May 2030

Related companies

Notified bodies

What AI Medical Technology AIM AB makes

AI Medical Technology AIM AB manufactures the Dermalyser, a device designed for non-invasive skin analysis and diagnostic procedures. This handheld instrument is primarily used in dermatological assessments, enabling precise measurements and evaluations of skin properties such as thickness, hydration, and texture.

The Dermalyser is classified under EU Medical Device Regulation as a Class IIa device and is registered in the EU’s eudamed database. The company is based in Sweden.

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 AI Medical Technology AIM AB manufacture?

AI Medical Technology AIM AB specializes in the Dermalyser, a handheld device for non-invasive skin analysis. It is primarily used in dermatology to assess skin properties like thickness, hydration, and texture without invasive procedures.

Where is AI Medical Technology AIM AB based?

The company is headquartered in Sweden, as indicated by its country designation.

Which regulatory registries list AI Medical Technology AIM AB’s devices?

The company’s devices, including the Dermalyser, are listed in the EU’s eudamed database, which is the official registry for medical devices under the EU Medical Device Regulation.

How are AI Medical Technology AIM AB’s devices classified?

The Dermalyser is classified as a Class IIa medical device under the EU Medical Device Regulation. This classification is based on its intended use for non-invasive skin analysis, which carries a moderate risk level requiring additional safety measures.

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

Information

Country
Sweden(from SRN)
Address
10, Brahegatan, Stockholm, Sweden
Website
aimedtech.com
Phone
+46 08 522 351 91
PRRC contact
Niya Thomas
EUDAMED SRN
SE-MF-000030500