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ALLERGIKA Pharma GmbH

Germany DE-MF-000016908 Last updated 21 Oct 2026

Devices
22
Registries
EUDAMED
FDA recalls
0

Catalogue22

EUDAMED certificates1

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

EUDAMED certificates (1)

Notified body 0044 1 certificate

  • 44911230005 Issued

    Quality management system EU MDR

    Issued
    7 May 2026
    Expires
    6 May 2031

Notified bodies

  • Notified body 0044

About

Special care for sensitive skin & mite protection for allergies ✓ Discover dermatologically tested Allergika products ➤ Inform now.

Translated from the manufacturer's own website. Source

What ALLERGIKA Pharma GmbH makes

The company manufactures encasing products, specifically the ALLERGIKA sensitive Encasing, which is designed for sensitive skin and mite protection for allergies. These products are intended to provide a barrier against allergens and irritants. The encasings are designed to be used on surfaces that come into contact with skin. They are made to help reduce exposure to allergens.

The company's products are classified as Class I devices and are listed in the Eudamed registry. The company is based in Germany. The devices are subject to regulatory oversight, and individual products may have undergone authorization procedures to ensure compliance with relevant standards.

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

Frequently asked questions

What type of products does ALLERGIKA Pharma GmbH manufacture?

The company manufactures encasing products, such as the ALLERGIKA sensitive Encasing, designed for sensitive skin and mite protection for allergies, to provide a barrier against allergens and irritants.

Where is ALLERGIKA Pharma GmbH based?

The company is based in Germany, as indicated by its country code DE.

Which regulatory registry lists ALLERGIKA Pharma GmbH's devices?

The company's devices are listed in the Eudamed registry, which is a database of medical devices.

How are ALLERGIKA Pharma GmbH's devices classified?

The company's devices, such as the ALLERGIKA sensitive Encasing, are classified as Class I devices, which undergo regulatory oversight to ensure compliance with relevant standards.

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

Information

Country
Germany
Address
58, Hans-Urmiller-Ring, Wolfratshausen, Germany
Phone
+49 8 171 42 25 7
PRRC contact
Michael Dr. Ernd
EUDAMED SRN
DE-MF-000016908