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Sign in to claim this brandPiomic 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
- Website
- www.piomic.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Adrian Meier
- EUDAMED SRN
- CH-MF-000013391
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| COMSfix | 01.0002 | EUDAMED | Class I | Active |
| COMStouch | 01.0001 | EUDAMED | Class I | Active |
| COMSfix | 01.0002 | EUDAMED | Class I | Active |
| COMSrefix | 01.0004 | EUDAMED | Class I | Active |
| COMS One basic | 01.0000 | EUDAMED | Class IIa | Active |
Related Companies
Authorised Representatives
- EUMEDIQ GmbH DE
Importers
Not available yet.
Notified Bodies
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Authorities
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