Pamark Group verkkokauppa
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
आवश्यक उत्पाद एक क्लिक दूर | पामार्क समूह
स्वास्थ्य देखभाल, सफाई और HoReCa पेशेवर उत्पाद एक ही स्थान पर आसानी से। उत्पादों की एक विस्तृत श्रृंखला और तेज़ डिलीवरी यह सुनिश्चित करती है कि आपको 99% डिलीवरी विश्वसनीयता के साथ वही मिले जो आपको चाहिए।
- Type
- Not established by any record (our catalog import lists it as distributor; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Finland
- Website
- https://pamark.fi
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ
What is established and what is not
No researcher review has been written for this company yet. No official record is on file. 1 other entry is not an official record: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-12. Domain registry record
Relationships
2 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Candidates, not confirmed
- pamark.fi: Website of this business. Source record
- LAERDAL MEDICAL AS: Named partner, country NO, passport https://hellofapartner.com/company/reg-979484488.
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)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.