Monidor Oy
Finland FI-MF-000007941 Last updated 21 Oct 2026
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- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Monidor Vitals Ref V017456
IV Screen Ref V004456
Monidrop Ref E001152, E001153
Monidrop W Ref V003453
EUDAMED certificates
SGS FIMKO OY 0598 1 certificate
- FI24/00000050 Supplemented
Quality management system EU MDR
- Issued
- 8 Jan 2026
- Expires
- 14 Aug 2027
- Valid from
- 9 Jan 2026
- Reason
- Other
Related companies
Notified bodies
- SGS FIMKO OY 0598
What Monidor Oy makes
Monidor Oy manufactures patient monitoring devices, including a wireless vital signs monitor (Monidor Vitals) for real-time tracking of physiological parameters, and an intravenous infusion screen (IV Screen) for visual confirmation of catheter placement. The company also produces infusion pumps (Monidrop and Monidrop W) designed for controlled delivery of fluids and medications in clinical settings.
The company’s product portfolio spans Class I, Class IIa, and Class IIb medical devices under EU regulations, with all relevant devices listed in the EU’s eudamed database. Monidor Oy is headquartered in Finland and adheres to applicable EU Medical Device Regulations (MDR) and regulatory requirements for its authorised devices.
Information
- Country
- Finland
- Address
- 3, Elektroniikkatie, Oulu, Finland
- Website
- monidor.com
- linkedin.com/company/monidor-oy
- facebook.com/Monidormedical
- [email protected]
- Phone
- +358 10 295 9063
- PRRC contact
- Seppo Puolitaival
- EUDAMED SRN
- FI-MF-000007941