Kiefel GmbH
Термоформовочное и сварочное оборудование для упаковочного, медицинского и автомобильного секторов.
Kiefel GmbH со штаб-квартирой во Фрайлассинге, Бавария, является лидером мирового рынка в области технологий термоформования и высокочастотной сварки пластиковых пленок, материалов на биологической основе и натуральных волокон. Компания Kiefel, входящая в группу Brückner Group, обслуживает производителей упаковки, медицинского оборудования, холодильников и автомобилей. Компания расширила свою деятельность на термоформование целлюлозного волокна для производства экологически чистой упаковки.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- Упаковка и полиграфия, Медицинские товары и расходники, Автозапчасти и аксессуары
- Markets
- Германия, Соединенные Штаты, Китай, Япония, Великобритания
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
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- registry-active-global (green), checked 2026-07-08 Handelsregister (North Data)
- domain-registered (green), checked 2026-08-02 Domain registry record
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Profiles
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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