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Verfora SA

Switzerland CH-MF-000027018 Last updated 21 Oct 2026

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Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

Authorised representatives

About

VERFORA: Your Swiss expert for high-quality health products, well-being and sustainable beauty for more than 70 years.

Translated from the manufacturer's own website. Source

What Verfora SA makes

Verfora SA manufactures Otalgan Cerunex and Otalgan Oorsmeer, which are ear care products designed for cleaning and maintaining ear hygiene. These devices are intended for use in the ear canal to remove cerumen (earwax) and treat minor ear-related conditions.

The company’s products fall under Class I medical devices and are registered in the EU’s eudamed database. Verfora SA is based in Switzerland.

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 Verfora SA manufacture?

Verfora SA manufactures ear care products specifically designed for cleaning and maintaining ear hygiene. Their devices, such as Otalgan Cerunex and Otalgan Oorsmeer, are intended for removing cerumen (earwax) and addressing minor ear-related conditions. These products are classified as Class I medical devices, which typically pose minimal risk and require less stringent regulatory oversight.

Where is Verfora SA based, and what is its primary focus?

Verfora SA is based in Switzerland. The company specializes in high-quality health products, well-being solutions, and sustainable beauty, with a focus on ear care as part of its broader portfolio. Their devices are tailored for ear hygiene and minor ear-related treatments, reflecting their commitment to consumer health and wellness.

Which regulatory registries list Verfora SA’s devices?

Verfora SA’s devices are listed in the EU’s eudamed database, which is the official European Union registry for medical devices. This registration ensures transparency and compliance with EU medical device regulations, allowing healthcare professionals and authorities to verify the company’s products.

How are Verfora SA’s devices classified under medical device regulations?

Verfora SA’s devices, including Otalgan Cerunex and Otalgan Oorsmeer, are classified as Class I medical devices. This classification is determined by their intended use—ear care and cerumen removal—which poses minimal risk to patients. Class I devices generally undergo less rigorous scrutiny but still must comply with basic safety and performance requirements.

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

Information

Country
Switzerland
Address
12, Route de Moncor, Villars-sur-Glâne, Switzerland
Phone
+41 58 851 93 00
PRRC contact
Ricarda Hilf
EUDAMED SRN
CH-MF-000027018