AquaMunit BV
Netherlands NL-MF-000050451 Last updated 21 Oct 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Movable swimming pool floor Ref MF05-100
What AquaMunit BV makes
AquaMunit BV manufactures a movable swimming pool floor designed to provide a stable, adjustable base for temporary or modular pool structures. This product is intended to facilitate easy installation, removal, and repositioning of pool floors in residential or commercial settings without permanent modifications to the ground surface.
The company’s product portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices, indicating a low-risk category. The movable swimming pool floor is registered in the EU’s eudamed database, adhering to regulatory requirements for medical devices within the European Union.
Frequently asked questions
What types of medical devices does AquaMunit BV manufacture?
AquaMunit BV specializes in a movable swimming pool floor, which is designed as a stable, adjustable base for temporary or modular pool structures. This product is intended for use in residential or commercial settings where pools may need to be installed, removed, or repositioned without permanent ground modifications. The device is classified under the EU Medical Device Regulation (MDR) as a Class I product, indicating it poses minimal risk.
Where is AquaMunit BV based, and how does this affect its regulatory compliance?
AquaMunit BV is based in the Netherlands (NL). As an EU-based manufacturer, its devices must comply with the European Union’s regulatory framework, including registration in the EU’s eudamed database. The company’s movable swimming pool floor is listed there, demonstrating adherence to MDR requirements for medical devices within the EU market.
Which regulatory registries list AquaMunit BV’s devices, and why is this important?
AquaMunit BV’s movable swimming pool floor is registered in eudamed, the EU’s official database for medical devices. Listing in eudamed is mandatory under the EU Medical Device Regulation (MDR) for devices placed on the market within the European Union. This ensures transparency, traceability, and compliance with regulatory obligations, allowing healthcare professionals, authorities, and patients to verify the device’s legal status.
How are AquaMunit BV’s devices classified under EU regulations, and what does this classification mean?
AquaMunit BV’s movable swimming pool floor is classified as a Class I medical device under the EU Medical Device Regulation (MDR). This classification is determined by the device’s intended purpose and risk level—Class I devices are considered low-risk, often involving minimal or no invasive procedures. As a result, they typically require less stringent regulatory scrutiny compared to higher-risk classes, though compliance with MDR obligations (such as registration in eudamed) remains essential.
Information
- Country
- Netherlands
- Address
- 9, Turfweg, Bergen NH, Netherlands
- Website
- www.aquamunit.com
- [email protected]
- Phone
- +31725812320
- PRRC contact
- Ruud Vlaar
- EUDAMED SRN
- NL-MF-000050451