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 EasyCut Plus Ref S4190004-XL
Stomacare Standard Ref 309-XL
Stomacare EasyOpener Plus Ref S3157204L-XXL
Stomacare EasyCut Plus Ref S4100004-M
Stomacare EasyCut Plus Ref S4190004-L
Stomacare Standard Ref G302R-XXXL
Stomacare EasyOpener Ref G306EOL-XXXXL
Stomacare Standard Ref 303R-L
Stomacare Standard Ref 303L-M
Stomy Ref 375.15-XXL
Stomacare Standard Ref 313L-XXXXL
Stomacare Standard HF Ref B301R-M
Clubycare Ref BA905L-25
Stomacare Standard Ref B313L-S
Stomacare HydroActive Ref 365-XL
Stomacare Standard Ref G312-XXXXL
Clubycare Ref BA905L-21
Stomacare HydroActive Ref 360-XXL
Stomacare Standard Ref B303L-XXL
Stomacare EasyOpener Plus Ref S3156004R-XXXXL
Stomacare Standard Ref B313R-M
Stomacare Faja para colostomía Ref 302PL-XXXL
QDM Stomacare halffabrikaat Ref B301MR-XXL
Stomacare Standard Ref B313L-XXXL
Stomacare HydroActive Ref 360-M
Stomacare Faja para colostomía Ref 302PL-L
Stomacare Standard Ref 303L-XXXXL
Stomy Ref 370.20-XXXL
Stomacare Faja para colostomía Ref 302PL-XXL
Stomacare EasyOpener Ref G312EOR-M
Stomacare Faja para colostomía Ref 305P-M
Stomacare Standard Ref 312-XXL
Clubycare Ref BA705R-28
Stomacare Faja para colostomía Ref 302PL-XL
Stomacare Standard Ref B303R-XXL
Stomy Ref 370.20-XXXXL
Stomacare Standard Ref G312-XXXL
Stomacare Standard Ref G302L-XXL
Stomacare Standard Ref G308-XXXL
Stomacare Standard Ref B303R-XL
Stomacare Standard Ref G302R-XL
Stomacare Standard HF Ref B305-M
Stomacare EasyOpener Ref B312EOR-XXXXL
Stomacare Standard Plus Ref S1158504-XXL
Stomacare Standard Ref B302R-XXXL
Stomacare Standard Ref G306-S
Stomacare Standard Ref 302L-M
Stomacare Standard Ref B302L-S
Stomacare Standard Ref G309-XL
Stomacare Standard HF Ref B301L-S
Showing 501-550 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