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Choose your advanced solution for soft tissue therapy The only tools on the market that come with an Online Learning Center Membership!
Choose your advanced solution for soft tissue therapy The only tools on the market that come with an Online Learning Center Membership! MobilityExpert Most Comprehensive IASTM System View more AdhesionTool Complete solution for soft tissue therapy View more GUA SHA Improved Performance through Stainless Steel View more
- Type
- Manufacturer
- Location
- Tartu linn, Estonia
- Founded
- 2013
- Website
- http://www.physioneers.com
- Categories
- Suprimentos médicos e de saúde
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)