Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Luciole Medical AG

Switzerland·CH-MF-000015856

Last updated September 18, 2026

What Luciole Medical AG makes

Luciole Medical AG manufactures reusable medical connectors and sensors designed for respiratory and anesthesia equipment, including cable assemblies for patch systems and compatibility adapters for specific manufacturer devices like General Electric, Dräger, and Philips. Their portfolio also includes disposable patch sensors and control units for monitoring respiratory parameters in clinical settings.

The company’s devices are classified under EU Medical Device Regulations as Class I and Class IIa, with all products registered in the EUDAMED database. Luciole Medical AG is based in Switzerland and adheres to regulatory requirements for medical devices within the European Union.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

Where is Luciole Medical AG based and what do they manufacture?

Luciole Medical AG is based in Switzerland. The company manufactures reusable medical connectors and sensors intended for use with respiratory and anesthesia equipment. Their product portfolio includes cable assemblies for patch systems, compatibility adapters for devices from manufacturers like General Electric, Dräger, and Philips, as well as disposable patch sensors and control units used for monitoring respiratory parameters in clinical settings.

How are the medical devices from Luciole Medical AG classified?

Under the European Union Medical Device Regulations, the devices produced by Luciole Medical AG are classified as either Class I or Class IIa. This classification system is used to determine the regulatory requirements and level of oversight necessary for each specific device based on its intended use and risk profile.

Where can I find the official registration information for these devices?

All medical devices manufactured by Luciole Medical AG are registered in the EUDAMED database. This is the European database on medical devices, which serves as the central repository for information regarding medical devices available within the European Union, ensuring transparency and regulatory compliance for the products listed.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Switzerland
Address
30, Baslerstrasse, Zurich (ZH), Switzerland
LinkedIn
—
Facebook
—
Phone
+41 43 343 96 04
PRRC Contact
Nicolas Bouche
EUDAMED SRN
CH-MF-000015856
FDA FEI Number
—
DUNS Number
—

Catalogue (11)

DeviceModel / ReferenceRegistriesClassStatus
RheoPatch Knob with cable 2.0, 2 meters 31020
EUDAMED
Class IActive
RheoPatch Knob with cable 2.0, 1 meter 31020
EUDAMED
Class IActive
RheoPatch Knob with cable 2.0, 3 meters 31020
EUDAMED
Class IActive
RheoConnect 1.0 General Electric Longer 22210
EUDAMED
Class IActive
RheoConnect 1.0 Dräger 22110
EUDAMED
Class IActive
RheoPatch Sensor 2.0 30020
EUDAMED
Class IActive
RheoLity 2.6 40026
EUDAMED
Class IIaActive
RheoConnect 1.0 General Electric 22210
EUDAMED
Class IActive
RheoLity 2.4 40024
EUDAMED
Class IIaActive
RheoConnect 1.0 Philips 22010
EUDAMED
Class IActive
RheoControl 10030
EUDAMED
Class IIaActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.