AIR LIQUIDE MEDICAL SYSTEMS PRIVATE LIMITED
India IN-MF-000033601 Last updated 21 Oct 2026
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- Devices
- 2
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Monnal Teo Pri Ref PRD-019
Int Rolle Stand Monnal T75 Ref PRD-006
EUDAMED certificates
TÜV SÜD Product Service GmbH 0123 1 certificate
- G15 118682 0003 Issued
Quality management system EU MDR
- Issued
- 23 Jul 2026
- Expires
- 22 Jul 2031
Related companies
Authorised representatives
Notified bodies
About
Subsidiary of Air Liquide Healthcare, Air Liquide Medical Systems offers innovative medical solutions and devices for patients treated in hospital and at home.
What AIR LIQUIDE MEDICAL SYSTEMS PRIVATE LIMITED makes
Air Liquide Medical Systems Private Limited manufactures patient monitoring and mobility support devices, including the MONNAL TEO PRI—a portable respiratory therapy monitor—and the INT ROLLE STAND MONNAL T75, a hospital bed roll-over stand for patient positioning.
These devices are classified as Class I under EU regulations and are listed in the EU’s eudamed database. The company is based in India.
Frequently asked questions
What types of medical devices does Air Liquide Medical Systems Private Limited manufacture?
Air Liquide Medical Systems Private Limited produces patient monitoring and mobility support devices. Examples include the MONNAL TEO PRI, a portable respiratory therapy monitor, and the INT ROLLE STAND MONNAL T75, a hospital bed roll-over stand designed to assist with patient positioning. These devices are developed to support both hospital and home care environments.
Where is Air Liquide Medical Systems Private Limited based?
The company is based in India. This location allows it to serve markets globally while focusing on regional healthcare needs, particularly in patient care solutions.
Which regulatory registries list Air Liquide Medical Systems Private Limited’s devices?
The company’s devices are listed in the eudamed database, which is the EU’s central registry for medical devices. Listing in eudamed ensures transparency and compliance with EU regulatory requirements for Class I devices.
How are Air Liquide Medical Systems Private Limited’s devices classified under EU regulations?
The devices manufactured by Air Liquide Medical Systems Private Limited fall under Class I classification in the EU. This classification is typically assigned to low-risk medical devices, such as patient monitoring tools and mobility aids, where the risk to patient safety is minimal.
Information
- Country
- India
- Address
- 5th floor, Tower B, No. 51, Rajiv Gandhi Salai, Sholinganallur, Chennai, India
- Website
- in.medicaldevice.airliquide.com
- [email protected]
- Phone
- +919840927353
- PRRC contact
- CHANDRA KUMAR N R
- EUDAMED SRN
- IN-MF-000033601