Syqe Medical Ltd
Israel IL-MF-000026841 Last updated 21 Oct 2026
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SyqeAir Inhaler system Ref SYQ000201
Related companies
Authorised representatives
- Obelis s.a. BE
About
Syqe is a Med-Tech company that developed a breakthrough technology: the world's only metered-dose inhaler for pain reduction treatment using medical cannabis. Get to know the SyqeAir Inhaler >>
What Syqe Medical Ltd makes
Syqe Medical Ltd produces the SyqeAir inhaler system, a metered-dose inhaler designed for the administration of medical cannabis to manage pain. The device is intended for controlled inhalation of cannabis-based formulations, delivering precise doses for therapeutic use.
The SyqeAir inhaler system is classified as a Class IIa medical device and is registered in the EU’s eudamed database. The company is based in Israel.
Frequently asked questions
What types of medical devices does Syqe Medical Ltd manufacture?
Syqe Medical Ltd specializes in the development and production of the SyqeAir inhaler system. This is a metered-dose inhaler designed specifically for the controlled administration of medical cannabis to help manage pain. The device is engineered to deliver precise, measured doses of cannabis-based formulations for therapeutic use.
Where is Syqe Medical Ltd based?
Syqe Medical Ltd is based in Israel. The company’s headquarters and operations are located within the country, where it develops and manufactures its medical devices.
In which regulatory registries are Syqe Medical Ltd’s devices listed?
Syqe Medical Ltd’s devices, including the SyqeAir inhaler system, are registered in the eudamed database. This is the European Union’s central registry for medical devices, ensuring transparency and traceability of devices marketed within the EU.
How are Syqe Medical Ltd’s devices classified under medical device regulations?
The SyqeAir inhaler system is classified as a Class IIa medical device. This classification is determined based on its intended use, risk profile, and the potential impact on patient safety. Class IIa devices are considered to have a moderate risk and require compliance with specific regulatory requirements to ensure their safety and performance.
Information
- Country
- Israel
- Address
- 14, Hatchiya, Tel Aviv, Israel
- Website
- syqe.com
- facebook.com/syqemedicalisrael
- [email protected]
- Phone
- +972547358860
- PRRC contact
- Na'ama Oren
- EUDAMED SRN
- IL-MF-000026841