ENGEL Austria GmbH
ENGEL, Avrupa'nın en büyük plastik enjeksiyon makinesi üreticisi ve küresel bir teknoloji lideridir…
ENGEL Avrupa'nın en büyük enjeksiyon kalıplama makinesi üreticisidir ve plastik işleme ekipmanlarında küresel bir teknoloji lideridir. Schwertberg fabrikası, 28 ila 5.500 ton kapama kuvvetine sahip kolonsuz zafer serisini ve büyük iki merdaneli ikili serisi makineleri üretmektedir. Müşteriler arasında 85 ülkedeki otomotiv Tier 1 tedarikçileri, tıbbi cihaz üreticileri ve paketleme şirketleri bulunmaktadır. Makinelerin yanı sıra tam kapsamlı otomasyon, takımlama ve IIoT çözümleri de mevcuttur.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Schwertberg, Austria
- Founded
- 1945
- Website
- engelglobal.com
- Categories
- Ambalaj ve Baskı Malzemeleri, Kişisel Bakım, Tıbbi ve Sağlık Malzemeleri
- Markets
- Almanya, Amerika Birleşik Devletleri, Çin, Japonya, Birleşik Krallık
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