EVTERPA COSMETIC & CO LTD
COSMÉTICA ORGÁNICA | ACEITE DE ROSA | ACEITE DE LAVANDA | AGUA DE ROSAS | AGUA DE LAVANDA | COSMÉTICA NATURAL | BULGARIA | VALLE DE TRACIA
COSMÉTICA ORGÁNICA | ACEITE DE ROSA | ACEITE DE LAVANDA | AGUA DE ROSAS | AGUA DE LAVANDA | COSMÉTICA NATURAL | BULGARIA | VALLE DE TRACIA | PRODUCTOR DE ACEITES ESENCIALES Y AGUAS FLORALES DE COSECHA PROPIA 2025 EVTERPA COSMETIC ofrece una amplia gama de servicios con respuesta rápida, precios competitivos y un fuerte enfoque en la satisfacción del cliente. Valoramos la flexibilidad, la innovación y la responsabilidad. Nuestro equipo está compuesto por expertos dedicados a los más altos estándares de investigación de laboratorio, control de calidad y desarrollo de productos. Dirigido por el Dr. Chernev, un distinguido graduado de la Universidad de Medicina de Plovdiv en 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
- Suministros médicos y sanitarios, Cuidado de la piel y cosmética, Iluminación y lámparas
- Markets
- Bulgaria
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)