Kiefel GmbH
Mesin thermoforming dan las untuk sektor pengemasan, medis dan otomotif.
Kiefel GmbH, yang berkantor pusat di Freilassing, Bavaria, adalah pemimpin pasar global dalam teknologi thermoforming dan pengelasan frekuensi tinggi untuk film plastik, bahan berbasis bio, dan serat alami. Bagian dari Grup Brückner, Kiefel melayani produsen pengemasan, perangkat medis, lemari es, dan otomotif. Perusahaan ini telah memperluas bidang thermoforming serat selulosa untuk aplikasi pengemasan yang berkelanjutan.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- Perlengkapan Pengemasan & Percetakan, Perlengkapan Medis & Kesehatan, Suku Cadang & Aksesori Kendaraan
- Markets
- Jerman, Amerika Serikat, Tiongkok, Jepang, Inggris Raya
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