Timik
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.
Tập đoàn Timik | Nhà phân phối và đối tác chuyển đổi MedTech của Bắc Âu
Timik Group là nhà phân phối và đối tác chuyển đổi MedTech hàng đầu Bắc Âu, cung cấp các giải pháp chăm sóc sức khỏe sáng tạo nhằm trao quyền cho người chăm sóc và bệnh nhân.
- 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
- Denmark
- Website
- https://timik.dk
- 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
- Listed as a distributor on a manufacturer's own site (record type: named-by-manufacturer) [our inference from comparing records, not an official record; status green] A manufacturer names this company as its distributor. effective since 2026-08-11. Aerogen Ltd distributor list
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
- timik.dk: Website of this business. Source record
- Aerogen Ltd: Named partner, country IE, passport https://hellofapartner.com/company/seed-aerogen.
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.