Planmed Oy
의료 및 건강 관리 용품, 핀란드
Planmed Oy는 핀란드 헬싱키에 본사를 둔 의료 및 건강 관리 용품 회사입니다. 공공 사업 등록부에 등재되어 있습니다.
- Type
- brand seeking distribution
- Location
- Helsinki, Finland
- Categories
- 의료 및 건강 관리 용품
Listed in a source registry
Verified facts
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- tax-filing-active (green), checked 2026-08-14 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- supervised-operator (green), checked 2026-08-14 Tukes register of operators (Finnish Safety and Chemicals Agency)
- public-contract-awarded (green), checked 2025-11-27 TED (Tenders Electronic Daily), EU public procurement award notices 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. EU와 EEA에서는 공공 발주자가 사기, 부패, 자금세탁으로 유죄가 확정된 입찰자와 최종 결정으로 세금 또는 사회보험료 체납이 확인된 입찰자를 반드시 배제해야 합니다. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-activity (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
- media-mention (green), checked 2026-07-15 Imaging Technology News
- registry-id-verified (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
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)