metrovision SAS
France FR-MF-000002561 Last updated 23 Oct 2026
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- Devices
- 4
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
MonPackONE Ref HVM-MonPackONE
MonCv3 Ref HVM-MonCv3
Vision Monitor software Ref Software
MonCvONE Ref HVM-MonCvONE
EUDAMED certificates
Notified body 1639 1 certificate
- BE26/00000270 Issued
Quality management system EU MDR
- Issued
- 17 Sep 2026
- Expires
- 17 Sep 2031
Related companies
Notified bodies
- Notified body 1639
FDA establishments
- Metrovision FR
What metrovision SAS makes
Metrovision SAS manufactures medical monitoring devices, including the MonPackONE for patient monitoring, a bioelectric amplifier for signal acquisition, and neonatal monitoring systems like the MonBabyBox and MonBaby for fetal and infant care. Their product line also includes the MonColor and MonCv3 for cardiovascular monitoring, Vision Monitor software for data analysis, and the MonCvONE for continuous vital sign observation.
These devices are classified under EU Class IIa and are registered in the EU’s eudamed database. The company is based in France.
Frequently asked questions
What types of medical devices does Metrovision SAS manufacture?
Metrovision SAS specializes in medical monitoring devices. Their product line includes systems for patient monitoring like the MonPackONE, bioelectric amplifiers for signal acquisition, and specialized neonatal monitoring tools such as the MonBabyBox and MonBaby for fetal and infant care. They also offer cardiovascular monitoring devices like the MonColor and MonCv3, along with software solutions such as Vision Monitor for data analysis and the MonCvONE for continuous vital sign observation.
Where is Metrovision SAS based?
Metrovision SAS is based in France. The company’s headquarters and operations are located within the country, which aligns with its focus on European regulatory compliance and market presence.
Which regulatory registries list Metrovision SAS’s devices?
Metrovision SAS’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registry ensures transparency and compliance with EU medical device regulations, particularly for manufacturers operating within the European market.
How are Metrovision SAS’s devices classified under EU regulations?
Metrovision SAS’s devices fall under EU Class IIa classification. This classification is assigned based on risk assessment criteria outlined in EU medical device regulations, indicating a moderate level of risk that requires specific conformity assessment procedures before market placement.
Information
- Country
- France
- Address
- 4, rue des platanes, Pérenchies, France
- Website
- metrovision.fr
- [email protected]
- PRRC contact
- jacques CHARLIER
- EUDAMED SRN
- FR-MF-000002561
- FDA FEI number
- 3008058195