Kiefel GmbH
Machines de thermoformage et de soudage pour les secteurs de l'emballage, du médical et de l'automobile.
Kiefel GmbH, dont le siège est à Freilassing, en Bavière, est un leader mondial du marché des technologies de thermoformage et de soudage à haute fréquence pour les films plastiques, les matériaux biosourcés et les fibres naturelles. Faisant partie du groupe Brückner, Kiefel est au service des fabricants d'emballages, de dispositifs médicaux, de réfrigérateurs et d'automobiles. L'entreprise s'est développée dans le thermoformage de fibres de cellulose pour des applications d'emballage durables.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- Emballage et fournitures d'impression, Fournitures médicales et de santé, Pièces et accessoires auto
- Markets
- Allemagne, États-Unis, Chine, Japon, Royaume-Uni
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