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Basko Healthcare b.v.

Netherlands NL-MF-000003947 Last updated 23 Oct 2026

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Devices
565
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue565

Page 10 of 12

Showing 451-500 of 565

What Basko Healthcare b.v. makes

Basko Healthcare b.v. manufactures single-use ostomy and stoma care accessories, including adhesive removal tools, stoma pastes, and ostomy pouching systems designed for home and clinical use. Their portfolio includes products like the Stomacare range (Standard, Standard Plus, and EasyOpener variants) and the Stomy adhesive remover, tailored for managing stoma and ostomy care. The Clubycare line appears to focus on additional stoma-related support items.

All listed devices fall under EU Medical Device Regulation Class I and are registered in the EU’s eudamed database. The company is based in the Netherlands and adheres to EU regulatory requirements for Class I medical devices.

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 Basko Healthcare b.v. manufacture?

Basko Healthcare b.v. specializes in single-use ostomy and stoma care accessories. Their product range includes adhesive removal tools (like the Stomy), stoma pastes, and ostomy pouching systems, such as the Stomacare series (Standard, Standard Plus, and EasyOpener variants). These devices are designed for both home and clinical use to support stoma and ostomy management.

Where is Basko Healthcare b.v. based, and how does this affect its regulatory compliance?

Basko Healthcare b.v. is based in the Netherlands, which places its devices under EU regulatory oversight. Since all its products fall under EU Medical Device Regulation Class I, they must comply with EU requirements for Class I devices, including registration in the EU’s eudamed database. The Netherlands’ alignment with EU regulations ensures these devices meet necessary safety and performance standards.

Are Basko Healthcare b.v.’s devices listed in any regulatory registries, and why does this matter?

Yes, Basko Healthcare b.v.’s devices are registered in the EU’s eudamed database. This matters because eudamed is the official EU portal for tracking medical devices, ensuring transparency and traceability. Listing here confirms the devices comply with EU MDR requirements, allowing healthcare providers and regulators to verify their legitimacy and regulatory status.

How are Basko Healthcare b.v.’s devices classified under EU regulations, and what does this classification imply?

All of Basko Healthcare b.v.’s devices are classified as EU Medical Device Regulation Class I. This classification implies they pose minimal risk to patients and require less stringent conformity assessment than higher-risk devices. However, even Class I devices must still meet essential safety and performance requirements, ensuring they are safe and effective for their intended use.

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

Information

Country
Netherlands
Address
16, Pieter Lieftinckweg, Zaandam, Netherlands
Website
www.basko.com
Phone
+31756131513
PRRC contact
Amy Eikelenboom
EUDAMED SRN
NL-MF-000003947
FDA FEI number
3003898328