Icare Finland Oy
Tonómetro de rebote OEM, medición de PIO sin contacto para oftalmología al por mayor.
Icare Finland Oy inventó el principio de tonometría de rebote y produce la familia de tonómetros Icare para medir la presión intraocular sin anestesia. Con sede en Espoo y filial del Grupo Revenio, la empresa vende a través de distribuidores de instrumentos oftálmicos en todo el mundo con autorizaciones CE y FDA.
- Type
- brand seeking distribution
- Location
- Espoo, Finland
- Founded
- 1999
- Website
- icare-world.com
- Categories
- Suministros médicos y sanitarios
- Markets
- Finlandia, Alemania, Reino Unido, Estados Unidos, Japón
Verified facts
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- tax-filing-active (green), checked 2026-08-14 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
- registry-id-verified (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-activity (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)