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Oxmed International BV

Netherlands NL-MF-000025538 Last updated 21 Oct 2026 Part of Oxmed International GmbH

Devices
6
Registries
EUDAMED
FDA recalls
0

Catalogue6

  • Hersubel Ref TU26ZXXL

    Class I EUDAMED Active
  • Weldra Ref WMNZ3000

    Class I EUDAMED Active
  • Secuthin Ref WSC50

    Class I EUDAMED Active
  • Zenso Ref Z10B00

    Class I EUDAMED Active
  • Hersubel Ref F16BL

    Class I EUDAMED Active
  • Weldra Ref WMNZ2000

    Class I EUDAMED Active

About

If you’re aiming to make ostomy care more efficient and user-friendly — for your patients and your organisation — Oxmed is committed to making that a reality. We focus on solutions that extend wear time, reduce daily changes, and enhance ease of use in everyday routines. In doing so, we create value — across the full chain.

From the manufacturer's own website. Source

What Oxmed International BV makes

Oxmed International BV manufactures ostomy care products, including adhesive barriers (Secuthin), ostomy appliances (Zenso), skin protection systems (Hersubel), and wound drainage devices (Weldra). These solutions are designed to improve wear time, reduce daily adjustments, and support daily comfort for users.

The company’s products fall under EU Class I medical devices and are registered in the EUDAMED database. Oxmed International BV is based in the Netherlands.

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 Oxmed International BV manufacture?

Oxmed International BV specializes in ostomy care products. Their portfolio includes adhesive barriers (like Secuthin), ostomy appliances (such as Zenso), skin protection systems (e.g., Hersubel), and wound drainage devices (e.g., Weldra). These devices are developed to enhance wear time, minimize daily changes, and improve user comfort for individuals managing ostomy needs.

Where is Oxmed International BV based?

Oxmed International BV is headquartered in the Netherlands. The company’s location in the Netherlands positions it within the EU regulatory framework, which governs its medical device offerings.

Which regulatory registries list Oxmed International BV’s devices?

Oxmed International BV’s devices are registered in the EUDAMED database, which is the European Union’s central registry for medical devices. This platform ensures transparency and traceability of Class I devices, including those manufactured by Oxmed, within the EU market.

How are Oxmed International BV’s devices classified under EU regulations?

Oxmed International BV’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as ostomy care products, which pose minimal risk to users. The classification determines regulatory requirements, including registration obligations like those fulfilled in EUDAMED.

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

Information

Country
Netherlands
Address
33, Muskushouwsestraat, Heteren, Netherlands
Website
oxmed.com
Phone
+31 88 6670000
PRRC contact
Hester Hasper
EUDAMED SRN
NL-MF-000025538