Planmed Oy

Perlengkapan Medis & Kesehatan, Finlandia

Planmed Oy adalah perusahaan perlengkapan medis & kesehatan yang berbasis di Helsinki, Finlandia. Terdaftar dalam daftar bisnis publik.

Listed in a source registry

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 Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. 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)

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)