EVTERPA COSMETIC & CO LTD
ORGANIC COSMETIC | ROSE OIL | LAVENDER OIL | ROSE WATER | LAVENDER WATER | NATURAL COSMETIC | BULGARIA | THRACIAN VALLEY | PRODUCER OF
ORGANIC COSMETIC | ROSE OIL | LAVENDER OIL | ROSE WATER | LAVENDER WATER | NATURAL COSMETIC | BULGARIA | THRACIAN VALLEY | PRODUCER OF ESSENTIAL OILS & FLORAL WATERS FROM OWN HARVEST 2025 EVTERPA COSMETIC offers a wide range of services with fast response, competitive pricing, and a strong focus on customer satisfaction. We value flexibility, innovation, and accountability. Our team is comprised of experts dedicated to the highest standards of laboratory research, quality control, and product development. Led by Dr. Chernev, a distinguished graduate of the 1995 Medical University of Plovdiv,
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Chirpan, Bulgaria
- Founded
- 1990
- Website
- evterpacosmetics.com
- Categories
- Medical & Healthcare Supplies, Skincare & Cosmetics, Lighting & Lamps
- 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)