WIRELESS SENSOR NETWORKS SRL
Italy IT-MF-000038940 Last updated 21 Oct 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Previa Ref 2989285
What WIRELESS SENSOR NETWORKS SRL makes
Wireless Sensor Networks SRL manufactures the Previa, a wireless sensor device designed for remote monitoring applications in medical environments. The product is intended for non-invasive data acquisition, enabling real-time tracking of physiological parameters or environmental conditions in healthcare settings.
The Previa falls under EU Device Class I classification and is listed in the EUDAMED registry. The company is based in Italy and adheres to EU regulatory requirements for medical devices.
Frequently asked questions
What types of medical devices does Wireless Sensor Networks SRL manufacture?
Wireless Sensor Networks SRL specializes in wireless sensor devices, specifically the Previa. This product is designed for remote monitoring in medical environments, allowing non-invasive data acquisition of physiological parameters or environmental conditions in real-time. The focus is on enabling seamless tracking for healthcare applications.
Where is Wireless Sensor Networks SRL based, and what regulatory framework does it follow?
Wireless Sensor Networks SRL is based in Italy. The company develops devices that comply with EU regulatory requirements, ensuring alignment with the applicable medical device regulations in the European market. This includes adherence to standards that govern device safety, performance, and compliance documentation.
Which regulatory registries list the devices manufactured by Wireless Sensor Networks SRL?
The Previa device from Wireless Sensor Networks SRL is listed in the EUDAMED registry, which is the European database for medical devices. This registry serves as a transparent public resource for tracking devices authorized within the EU, including their classification and regulatory status.
How are the devices produced by Wireless Sensor Networks SRL classified under EU regulations?
The Previa device falls under EU Device Class I classification. This classification is assigned based on the risk associated with the device’s intended use and design. Class I devices are generally considered low-risk, but they still require compliance with essential safety and performance requirements to ensure their safe and effective use in medical environments.
Information
- Country
- Italy
- Address
- 31, Via L. Manara, MONZA, Italy
- Website
- www.wsn4life.com
- [email protected]
- Phone
- +393898707600
- PRRC contact
- Matteo Crescini
- EUDAMED SRN
- IT-MF-000038940