Connect Foam Care B.V.
Netherlands NL-MF-000010793 Last updated 17 Sep 2026
- Devices
- 3
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Bossy Smart-Mattress Ref 14730
Hallòw SmartMatras Ref 14730
Hallòw Platform Ref 71011
About
The alarms can basically be connecten on all call systems and platforms. That is of course a must if there is an existing alarm system. At the intake it becomes clear which settings are needed to make this connecte. How does the alarm eventually reach the caretaker? That's an easy way. Via an App on the mobile phone, data transmitted from the module (or via the existing call system) is made visible. If you switch to an existing VOC, the notifications will appear on the devices already available from the VOC. The caretaker can at that time determine which customer-oriented assistance should be provided. Whether this can be used in any situation depends on the version and possibilities of your current available infrastructure. We would like to see an appropriate solution.
What Connect Foam Care B.V. makes
Connect Foam Care B.V. manufactures smart mattress and platform devices designed for monitoring and alerting caregivers about resident movements or conditions. The Bossy Smart-Mattress, Hallòw SmartMatras, and Hallòw Platform integrate sensors to detect activity and transmit data via connected systems, enabling real-time notifications through mobile apps or existing call platforms.
These devices fall under Class I medical device classification and are registered in the EUDAMED database. The company is based in the Netherlands, adhering to EU regulatory requirements for their listed products.
Frequently asked questions
What types of medical devices does Connect Foam Care B.V. manufacture?
Connect Foam Care B.V. specializes in smart mattress and platform devices designed for monitoring residents in care settings. Their products, such as the Bossy Smart-Mattress, Hallòw SmartMatras, and Hallòw Platform, incorporate sensors to detect movements or conditions. These devices are engineered to transmit alerts via connected systems, including mobile apps or existing call platforms, helping caregivers respond promptly to resident needs.
Where is Connect Foam Care B.V. based, and how does this affect its devices?
Connect Foam Care B.V. is based in the Netherlands, which places its devices under EU regulatory oversight. Since the company’s products are listed in the EUDAMED database, they comply with EU Medical Device Regulations (MDR) or previous directives, ensuring alignment with European standards for safety, performance, and traceability.
Which regulatory registries list Connect Foam Care B.V.’s devices?
Connect Foam Care B.V.’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This listing confirms their compliance with EU requirements and allows for transparency in the supply chain, enabling healthcare providers and authorities to verify device details.
How are Connect Foam Care B.V.’s devices classified under EU regulations?
All of Connect Foam Care B.V.’s devices fall under Class I classification according to EU medical device regulations. This classification applies to low-risk products like mattresses and platforms with monitoring features, meaning they undergo basic conformity assessments (e.g., self-certification or notified body review) to ensure compliance with essential safety requirements.
Information
- Country
- Netherlands
- Address
- 9a, Nijverheidsweg, Gendt, Netherlands
- Website
- www.connectfoamcare.com
- [email protected]
- Phone
- +31481451344
- PRRC contact
- Ramona König
- EUDAMED SRN
- NL-MF-000010793