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Elija su solución avanzada para la terapia de tejidos blandos. ¡Las únicas herramientas en el mercado que vienen con una membresía del Centro de aprendizaje en línea! móvil
Elija su solución avanzada para la terapia de tejidos blandos. ¡Las únicas herramientas en el mercado que vienen con una membresía del Centro de aprendizaje en línea! MobilityExpert Sistema IASTM más completo Ver más AdhesionTool Solución completa para terapia de tejidos blandos Ver más GUA SHA Rendimiento mejorado a través del acero inoxidable Ver más
- Type
- Manufacturer
- Location
- Tartu linn, Estonia
- Founded
- 2013
- Website
- http://www.physioneers.com
- Categories
- Suministros médicos y sanitarios
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-07-27 Domain registry record
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2013-03-13 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2013-03-13 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-manufacturer (green), checked 2026-08-06 e-Äriregister (teatatud tegevusalad)
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- media-mention (green), checked 2026-03-05 med24.ee
- registry-id-verified (green), checked 2026-07-27 e-Business Register (e-Ariregister), Centre of Registers and Information Systems (RIK)
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- tax-filing-active (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
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)