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.
Sản phẩm cần thiết chỉ với một cú nhấp chuột | Nhóm Pamark
Chăm sóc sức khỏe, làm sạch và các sản phẩm chuyên nghiệp HoReCa dễ dàng ở một nơi. Một loạt các sản phẩm và giao hàng nhanh chóng đảm bảo rằng bạn nhận được chính xác những gì bạn cần, với độ tin cậy giao hàng 99%.
- 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
- Vật tư y tế và chăm sóc sức khỏe
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.