EVTERPA COSMETIC & CO LTD
BIO-KOSMETIK | ROSENÖL | LAVENDELÖL | ROSENWASSER | LAVENDELWASSER | NATÜRLICHE KOSMETIK | BULGARIEN | THRAKISCHES TAL | HERSTELLER VON
BIO-KOSMETIK | ROSENÖL | LAVENDELÖL | ROSENWASSER | LAVENDELWASSER | NATÜRLICHE KOSMETIK | BULGARIEN | THRAKISCHES TAL | HERSTELLER VON ÄTHERISCHEN ÖLEN UND BLUMENWASSER AUS EIGENER ERNTE 2025 EVTERPA COSMETIC bietet eine breite Palette von Dienstleistungen mit schneller Reaktion, wettbewerbsfähigen Preisen und einem starken Fokus auf Kundenzufriedenheit. Wir legen Wert auf Flexibilität, Innovation und Verantwortung. Unser Team besteht aus Experten, die sich den höchsten Standards der Laborforschung, Qualitätskontrolle und Produktentwicklung widmen. Unter der Leitung von Dr. Chernev, einem angesehenen Absolventen der Medizinischen Universität Plovdiv im Jahr 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
- Medizin- & Gesundheitsbedarf, Hautpflege & Kosmetik, Beleuchtung & Lampen
- Markets
- Bulgarien
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)