Basko Healthcare b.v.
Netherlands NL-MF-000003947 Last updated 23 Oct 2026
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- Devices
- 565
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Stomacare Standard Ref 303L-XXL
Stomacare Standard Ref G313L-XXXL
Stomacare Standard Plus Ref S1196004-S
Stomacare Standard Ref 303L-S
Stomacare Standard Plus Ref S1107204-XXXXL
Stomacare Faja para colostomía Ref 303PL-XL
Stomacare Standard Ref B308-XL
Stomacare Standard Ref 307-L
Stomacare Standard Ref B306-S
Stomacare Standard HF Ref G301R-XXXL
Stomacare Standard Ref 308-XL
Clubycare Ref BA705L-27
Stomacare Standard Ref 302R-XXXXL
Stomy Ref 370.20-M
Stomacare Standard HF Ref G301R-M
Stomy Ref 370.20-S
Stomacare Standard Ref 306-XL
Stomacare EasyOpener Plus Ref S3157204L-XXXXL
Stomacare Standard Ref G313R-M
Stomacare Standard Ref 313L-XXL
Stomacare Standard Ref B302R-M
Clubycare Ref BA905R-21
Stomacare Standard Ref G313L-XL
Stomacare Standard Ref B303R-L
Clubycare Ref BA908L-14
Stomacare Standard Ref G313R-L
Stomacare Standard Plus Ref S1107204-XXL
Stomacare Standard Ref G308-S
Stomacare Standard Ref B308-XXL
Stomy Ref 375.15-L
Stomacare Standard Ref B307-L
Stomacare Standard Ref G307-S
Stomacare HydroActive Ref 365-S
Stomacare Standard Ref G303R-XXXL
Stomacare Standard Ref B313L-XXXXL
QDM Stomacare halffabrikaat Ref B301ML-XXL
Stomacare Faja para colostomía Ref 303PL-L
Stomacare EasyOpener Ref 307EOL-M
Clubycare Ref BA905L-19
Clubycare Ref BA705R-18
Stomacare Standard Plus Ref S1196004-L
Stomacare EasyOpener Ref B312EOR-M
Stomacare EasyOpener Plus Ref S3158504L-XXL
Stomacare Faja para colostomía Ref 306P-XL
Stomacare EasyOpener Plus Ref S3156004R-S
Stomacare Standard Plus Ref S1106004-S
Stomacare Standard Ref 302L-XXL
Stomacare Standard Ref G312-S
Stomacare EasyCut Plus Ref S4190004-S
Stomacare Standard HF Ref 301R-XXL
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.
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.
Information
- Country
- Netherlands
- Address
- 16, Pieter Lieftinckweg, Zaandam, Netherlands
- Website
- www.basko.com
- [email protected]
- Phone
- +31756131513
- PRRC contact
- Amy Eikelenboom
- EUDAMED SRN
- NL-MF-000003947
- FDA FEI number
- 3003898328