Screentec Oy
Inactive in EUDAMED since 2024Finlandfrom SRN EUDAMED FDA SRN FI-MF-000011935 FEI 3013164281
Inactive. This company's EUDAMED actor record is marked inactive. Check the current status before ordering.
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Screentec Roiskeen-/nesteenpitävä kertakäyttöinen suu-nenäsuojus (tyyppi IIR, ei steriili), 50kpl Ref 06429810668035
Regimes: CE MDR, withdrawn Registry: EUDAMEDScreentec Roiskeen-/nesteenpitävä kertakäyttöinen suu-nenäsuojus (tyyppi IIR, ei steriili), 10 kpl Ref 06429810668004
Regimes: CE MDR, withdrawn Registry: EUDAMED
Company details
- EUDAMED SRN
- FI-MF-000011935
- FDA FEI number
- 3013164281
- EU VAT number
- FI07570954
- EUDAMED status
- Inactive since 2024
- EUDAMED registered name
- Screentec Oy
- Registered address
- 2, Konekuja, 90620, Oulu, Finland
- Website
- www.screentec.com/
- [email protected]
- Phone
- +358 85612000
- PRRC contact
- Jaana Kananen
Frequently asked questions
How many devices does Screentec Oy have in the registry?
The registry currently lists 2 devices for Screentec Oy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Screentec Oy's devices?
Among its 2 most recently registered devices, Screentec Oy has devices listed in EUDAMED (2 devices).
What risk classes do Screentec Oy's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Screentec Oy's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Screentec Oy in the registry?
The most recently registered devices listed for Screentec Oy include Screentec Roiskeen-/nesteenpitävä kertakäyttöinen suu-nenäsuojus (tyyppi IIR, ei steriili), 50kpl and Screentec Roiskeen-/nesteenpitävä kertakäyttöinen suu-nenäsuojus (tyyppi IIR, ei steriili), 10 kpl.