ENGEL Austria GmbH
ENGEL to największy w Europie producent wtryskarek i światowy lider technologii…
ENGEL jest największym w Europie producentem wtryskarek i światowym liderem technologii w zakresie urządzeń do przetwórstwa tworzyw sztucznych. Fabryka w Schwertberg produkuje bezkolumnowe maszyny serii Victor oraz duże dwupłytowe maszyny serii Duo o sile zwarcia od 28 do 5500 ton. Do klientów należą dostawcy branży motoryzacyjnej Tier 1, producenci urządzeń medycznych i firmy opakowaniowe w 85 krajach. Kompletna automatyzacja, narzędzia i rozwiązania IIoT dostępne wraz z maszynami.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Schwertberg, Austria
- Founded
- 1945
- Website
- engelglobal.com
- Categories
- Materiały do pakowania i drukowania, Opieka osobista, Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Niemcy, Stany Zjednoczone, Chiny, Japonia, Wielka Brytania
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
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment