Arabian Ethicals
Надежный дистрибьютор медицинской фармацевтической и косметической продукции
Мы управляем соблюдением импортных требований и дистрибуцией медико-биологических продуктов и средств по уходу за кожей. Мы поставляем продукцию напрямую государственным проектам здравоохранения и аптечным сетям.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Dubai, United Arab Emirates
- Founded
- 1977
- Website
- arabianethicals.ae
- Categories
- Медицинские товары и расходники, Уход за кожей и косметика
- Markets
- ОАЭ
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)