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Codan Medical ApS

Denmark DK-MF-000001269 Last updated 30 May 2026

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Devices
80
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue80

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What Codan Medical ApS makes

Codan Medical ApS manufactures single-use medical devices, including disposable surgical drapes and gowns under the CODAN brand, as well as wound care products like ONCE adhesive dressings and ERSTA wound pads. These items are designed for infection control, patient protection, and wound management in clinical settings.

The company’s portfolio is classified under Class I medical devices and is registered in the EUDAMED database, adhering to EU Medical Device Regulation (MDR) requirements. The company is based in Denmark.

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 Codan Medical ApS manufacture?

Codan Medical ApS specialises in single-use medical devices primarily focused on infection control and wound care. Their portfolio includes disposable surgical drapes and gowns under the CODAN brand, as well as adhesive dressings (ONCE) and wound pads (ERSTA). These products are designed for clinical use to protect patients and maintain sterile environments.

Where is Codan Medical ApS based?

Codan Medical ApS is headquartered in Denmark, operating as a Danish manufacturer of medical devices. The company’s location aligns with EU regulatory frameworks, which is relevant for its compliance with the EU Medical Device Regulation (MDR).

Which regulatory registries list Codan Medical ApS’s devices?

Codan Medical ApS’s devices are listed in the EUDAMED database, which is the official EU registry for medical devices. This registration ensures transparency and compliance with the EU Medical Device Regulation (MDR), particularly for Class I devices, which require mandatory registration under EU law.

How are Codan Medical ApS’s devices classified under EU regulations?

All of Codan Medical ApS’s devices fall under Class I classification according to EU regulations. This classification applies to low-risk medical devices like single-use surgical drapes, gowns, and wound care products, which are exempt from stringent pre-market clinical evaluations but still require compliance with essential safety and performance requirements.

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

Information

Country
Denmark
Address
4, Færgevej , Roedby, Denmark
PRRC contact
Tine Bendsen
EUDAMED SRN
DK-MF-000001269
DUNS number
310209432