EVTERPA COSMETIC & CO LTD
COSMÉTICO ORGÂNICO | ÓLEO DE ROSA | ÓLEO DE LAVANDA | ÁGUA DE ROSAS | ÁGUA DE LAVANDA | COSMÉTICO NATURAL | BULGÁRIA | VALE TRÁCIA |
COSMÉTICO ORGÂNICO | ÓLEO DE ROSA | ÓLEO DE LAVANDA | ÁGUA DE ROSAS | ÁGUA DE LAVANDA | COSMÉTICO NATURAL | BULGÁRIA | VALE TRÁCIA | PRODUTOR DE ÓLEOS ESSENCIAIS E ÁGUAS FLORAIS DE COLHEITA PRÓPRIA 2025 A EVTERPA COSMETIC oferece uma ampla gama de serviços com resposta rápida, preços competitivos e forte foco na satisfação do cliente. Valorizamos flexibilidade, inovação e responsabilidade. Nossa equipe é composta por especialistas dedicados aos mais altos padrões de pesquisa laboratorial, controle de qualidade e desenvolvimento de produtos. Liderado pelo Dr. Chernev, um distinto graduado da Universidade Médica de Plovdiv de 1995,
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Chirpan, Bulgaria
- Founded
- 1990
- Website
- evterpacosmetics.com
- Categories
- Suprimentos médicos e de saúde, Cuidados com a pele e cosméticos, Iluminação e luminárias
- Markets
- Bulgária
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
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
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)