INOSYSTEMS
France FR-MF-000011282 Last updated 22 Oct 2026
- Devices
- 70
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
External Power Supply Enclosure Ref IN000340
Monnal Ino Advanced Ref IN000357
Monnal Ino Advanced Ref IN000345
Ino Monitoring 15mm Ref IN000302
NO gas hose (3m) Ref IN000313
NO gas hose (1.1m) Ref IN000329
Monnal Ino Advanced Ref IN000358
Monnal Ino Advanced Ref IN000356
Nebulisation filter Ref IN000148
Monnal Ino Advanced Ref IN000324
Monnal Ino Advanced Ref IN000350
iNO Patient Kit, Bunnell Ref IN000127
SoKINOX Ref IN000279
SoKINOX Ref IN000110
Monnal Ino Advanced Ref IN000327
SoKINOX Ref IN000264
iNO PATIENT KIT NEXT/ADVANCED Ref IN000299
Monnal iNO Ref IN000347
Sokinox Next Ref IN000322
Sokinox Next Ref IN000316
Showing 51-70 of 70
What INOSYSTEMS makes
Inosystems manufactures respiratory and monitoring devices including the INO Monitoring Luer Elbow Pack, Mobile Cart, MONNAL iNO, High Flow Sensor, INO Additional Adapters, SOKINOX Next, SOKINOX, Flow Sensor Bunnell Next/Adv, and INO Transport Clamp.
These devices are classified as Class I, Class IIa, and Class IIb medical devices and are listed in the EUDAMED database. The company is based in France.
Frequently asked questions
What types of devices does Inosystems manufacture?
Inosystems manufactures respiratory and monitoring devices, including the INO Monitoring Luer Elbow Pack, Mobile Cart, MONNAL iNO, High Flow Sensor, INO Additional Adapters, SOKINOX Next, SOKINOX, Flow Sensor Bunnell Next/Adv, and INO Transport Clamp, as these are the specific products listed in the provided device data.
Where is Inosystems based?
Inosystems is based in France, as explicitly stated in the country field (FR) and confirmed in the summary section of the device data.
In which regulatory registry are Inosystems' devices listed?
Inosystems' devices are listed in the EUDAMED database, as directly indicated in the LISTED IN field and reiterated in the summary, which confirms their inclusion in this European regulatory system.
How are Inosystems' devices classified under medical device regulations?
Inosystems' devices are classified as Class I, Class IIa, and Class IIb medical devices, as specified in the DEVICE CLASSES field and repeated in the summary, reflecting their risk-based categorization under EU regulations.
Information
- Country
- France
- Address
- 7, RUE GEORGES BESSE, ANTONY Cedex, France
- Website
- inosystems.fr
- [email protected]
- EUDAMED SRN
- FR-MF-000011282
- FDA FEI number
- 3019771924