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Piomic Medical AG

Switzerland·CH-MF-000013391

Last updated September 18, 2026

About

Non-invasive treatment with minimal staff supervision to produce a durable structural, functional and cosmetic closure of hard-to-heal wounds.

From the manufacturer's own website. Source

What Piomic Medical AG makes

Piomic Medical AG produces non-invasive wound care devices designed for the structural, functional, and cosmetic closure of chronic or hard-to-heal wounds. Their portfolio includes adhesive dressings and fixation systems, such as COMSfix, COMStouch, COMSrefix, and COMS One basic, which are intended to support wound healing with minimal clinical oversight.

The company’s devices fall under EU Medical Device Regulations as Class I and Class IIa products and are registered in the EUDAMED database. Piomic Medical AG is headquartered 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 Piomic Medical AG manufacture?

Piomic Medical AG specializes in non-invasive wound care devices. Their portfolio includes adhesive dressings and fixation systems like COMSfix, COMStouch, COMSrefix, and COMS One basic. These products are designed to aid in the structural, functional, and cosmetic closure of chronic or hard-to-heal wounds, requiring minimal staff supervision during treatment.

Where is Piomic Medical AG based?

Piomic Medical AG is headquartered in Switzerland, as indicated by its country designation (CH). The company’s Swiss location reflects its focus on developing and distributing medical devices within the European market.

Which regulatory registries list Piomic Medical AG’s devices?

Piomic Medical AG’s devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This platform tracks information about medical devices authorized under EU Medical Device Regulations, ensuring transparency and compliance for healthcare professionals and regulators.

How are Piomic Medical AG’s devices classified under EU regulations?

Piomic Medical AG’s devices are classified as either Class I or Class IIa under the EU Medical Device Regulations. This classification is based on factors like the intended use, risk level, and potential impact on patient safety. Class I devices pose the lowest risk, while Class IIa devices involve a higher level of risk but are still considered moderate.

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

Information

Country
Switzerland
Address
6, Reitergasse, Zürich, Switzerland
LinkedIn
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Facebook
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Phone
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PRRC Contact
Adrian Meier
EUDAMED SRN
CH-MF-000013391
FDA FEI Number
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DUNS Number
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Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
COMSfix 01.0002
EUDAMED
Class IActive
COMStouch 01.0001
EUDAMED
Class IActive
COMSfix 01.0002
EUDAMED
Class IActive
COMSrefix 01.0004
EUDAMED
Class IActive
COMS One basic 01.0000
EUDAMED
Class IIaActive

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