Sharkmedical
Sharkmedical - Proudly serving you
Product categories Military NAR, TacMed, C-A-T and other tactical first aid quality professional products for use by the military. Read more Police/tactical first aid NAR, TacMed, C-A-T and other high-quality professional products for police and tactical first aid. Read more First aid PAX backpacks, LIFEPAK defibrillators, Blizzard
- Type
- distributor seeking brands
- Location
- Finland
- Website
- https://sharkmed.fi
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Finland
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- public-contract-awarded (green), checked 2026-06-26 TED (Tenders Electronic Daily), EU public procurement award notices Hier draagt de gunning ook een controle van een ander: in de EU en de EER moet een publieke inkoper inschrijvers uitsluiten die zijn veroordeeld voor fraude, corruptie of witwassen, en degenen bij wie een definitief besluit belasting of premieschulden heeft vastgesteld. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-id-verified (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-active-global (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)
- 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)
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)