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Euromed A/S

Country not established

Devices
4

What Euromed A/S makes

Euromed A/S makes wound care products, including SURESKIN STANDARD, BORDER, and THIN devices. These are types of wound dressings or skin contact devices.

The company's portfolio is regulated under device class U and is listed in the FDA 510k registry. Euromed A/S is based in the US.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Sureskin Standard, Border, And Thin Ref K963039

    Unclassified
    Active 510(k) 510(k) —
  • Sureskin Standard Ref K960394

    Unclassified
    Active 510(k) 510(k) —
  • Sureskin Thin Ref K960404

    Unclassified
    Active 510(k) 510(k) —
  • Sureskin Border Ref K960393

    Unclassified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does Euromed A/S have in the registry?

The registry currently lists 4 devices for Euromed A/S. Devices recorded under merged duplicate company entries are counted once.

Which registries list Euromed A/S's devices?

Among its 4 most recently registered devices, Euromed A/S has devices listed in FDA 510(k) (4 devices).

What are the newest devices from Euromed A/S in the registry?

The most recently registered devices listed for Euromed A/S include SURESKIN STANDARD, BORDER, AND THIN, SURESKIN STANDARD, SURESKIN THIN and SURESKIN BORDER.

Generated automatically from registry data and not verified by a human reviewer.