EVTERPA COSMETIC & CO LTD
ORGANİK KOZMETİK | GÜL YAĞI | LAVANTA YAĞI | GÜL SUYU | LAVANTA SUYU | DOĞAL KOZMETİK | BULGARİSTAN | TRAKYA VADİSİ | KENDİ HASATINDAN
ORGANİK KOZMETİK | GÜL YAĞI | LAVANTA YAĞI | GÜL SUYU | LAVANTA SUYU | DOĞAL KOZMETİK | BULGARİSTAN | TRAKYA VADİSİ | KENDİ HASATINDAN UÇUCU YAĞLAR VE ÇİÇEK SULARI ÜRETİCİSİ 2025 EVTERPA KOZMETİK, hızlı yanıt, rekabetçi fiyatlandırma ve müşteri memnuniyetine güçlü bir odaklanma ile geniş bir hizmet yelpazesi sunmaktadır. Esnekliğe, yeniliğe ve sorumluluğa değer veriyoruz. Ekibimiz, laboratuvar araştırması, kalite kontrol ve ürün geliştirmede en yüksek standartlara kendini adamış uzmanlardan oluşur. 1995 yılında Plovdiv Tıp Üniversitesi'nin seçkin bir mezunu olan Dr. Chernev'in liderliğinde,
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Chirpan, Bulgaria
- Founded
- 1990
- Website
- evterpacosmetics.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Cilt Bakımı ve Kozmetik, Aydınlatma ve Lambalar
- Markets
- Bulgaristan
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)