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Contura International A/S

Denmark·DK-MF-000002018

Last updated September 17, 2026

What Contura International A/S makes

Contura International A/S manufactures urethral bulking systems and related components, including the Bulkamid® Needle, Bulkamid® Rotatable Sheath, Bulkamid® Hydrogel, and the Bulkamid® Urethral Bulking System, as well as the Arthrosamid® product for joint treatment.

The company's devices are classified as Class I, Class IIa, and Class IIb medical devices and are listed in the EUDAMED database; Contura International A/S is based in Denmark (DK).

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Contura International A/S manufacture?

Contura International A/S manufactures urethral bulking systems and related components, including the Bulkamid® Needle, Bulkamid® Rotatable Sheath, Bulkamid® Hydrogel, and the Bulkamid® Urethral Bulking System, as well as the Arthrosamid® product for joint treatment, based solely on the provided device data.

Where is Contura International A/S based?

Contura International A/S is based in Denmark, as indicated by the country code DK in the provided data, which specifies the company's location without referencing any operational details beyond that.

Which regulatory registry lists Contura International A/S's devices?

Contura International A/S's devices are listed in the EUDAMED database, as explicitly stated in the LISTED IN field of the provided data, which identifies the registry where their devices are registered.

How are Contura International A/S's devices classified?

Contura International A/S's devices are classified as Class I, Class IIa, and Class IIb medical devices, according to the DEVICE CLASSES field in the provided data, which specifies the risk-based classification levels applicable to their products.

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

Information

Country
Denmark
Address
23, Sydmarken, Soeborg, Denmark
Website
contura.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
—
EUDAMED SRN
DK-MF-000002018
FDA FEI Number
3005111102
DUNS Number
—

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Bulkamid® Needle 10001491
EUDAMED
Class IIaActive
Bulkamid® Rotatable Sheath 10047
EUDAMED
Class IActive
Bulkamid® Hydrogel 50009
EUDAMED
Class IIbActive
Bulkamid® Urethral Bulking System 50012
EUDAMED
Class IIbActive
Arthrosamid® 50020
EUDAMED
Class IIbActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Contura International A/S US