EVTERPA COSMETIC & CO LTD
KOSMETIK ORGANIK | MINYAK MAWAR | MINYAK LAVENDER | AIR MAWAR | AIR LAVENDER | KOSMETIK ALAMI | BULGARIA | LEMBAH THRACIA | PRODUSEN MINYAK
KOSMETIK ORGANIK | MINYAK MAWAR | MINYAK LAVENDER | AIR MAWAR | AIR LAVENDER | KOSMETIK ALAMI | BULGARIA | LEMBAH THRACIA | PRODUSEN MINYAK ESENSIAL & AIR BUNGA DARI PANEN SENDIRI TAHUN 2025 EVTERPA COSMETIC menawarkan berbagai layanan dengan respon cepat, harga kompetitif, dan fokus kuat pada kepuasan pelanggan. Kami menghargai fleksibilitas, inovasi, dan akuntabilitas. Tim kami terdiri dari para ahli yang berdedikasi pada standar tertinggi penelitian laboratorium, kendali mutu, dan pengembangan produk. Dipimpin oleh Dr. Chernev, lulusan terkemuka dari Universitas Kedokteran Plovdiv tahun 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
- Perlengkapan Medis & Kesehatan, Perawatan Kulit & Kosmetik, Penerangan & Lampu
- 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)