Derma art, proizvodnja in storitve d.o.o.
スロベニアの工業製造業者および輸出業者
ダーマアート、storitve d.o.o.のproizvodnja Sloexport によりその他の製造部門に上場されています。そのディレクトリ プロファイルには、Derma Art d.o.o を含むオペレーションが記述されています。は医療機器の開発・製造を行っている企業です。製造施設はスロベニアのブレジツェにあり、ISO13485 認証を取得しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Brežice, Slovenia
- Website
- https://dermaart.si
- Categories
- 医薬品製造, 医療およびヘルスケア用品
- Markets
- スロベニア, オーストリア, ドイツ, イタリア, クロアチア
Listed in a source registry
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
- domain-registered (green), checked 2026-08-08 Domain registry record
- 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
- lei-active (green), checked 2026-08-08 GLEIF
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
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)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)