RemeCure APS
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.
المكملات الغذائية المكثفة والمستحضرات الصيدلانية والأجهزة الطبية التي تم تطويرها في الدنمارك
RemeCure هي شركة أوروبية متخصصة في تصنيع المكملات الغذائية ذات العلامات التجارية الخاصة والمتخصصة في تصنيع العلكة والأقراص والكبسولات والبروبيوتيك والسوائل وتصنيع العقود الغذائية. خدمة الرعاية الصحية والعلامات التجارية الصيدلانية في جميع أنحاء العالم.
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Denmark
- Website
- https://remecure.com
- Categories
- تصنيع الأدوية, اللوازم الطبية والرعاية الصحية, المكملات الغذائية والعافية
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 2026-08-02. Domain registry record
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)
Goods family established: اللوازم الطبية والرعاية الصحية (the company's own text), المكملات الغذائية والعافية (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category تصنيع الأدوية: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.