Kiefel GmbH
Macchine per termoformatura e saldatura per il settore packaging, medicale e automobilistico.
Kiefel GmbH, con sede a Freilassing, in Baviera, è leader di mercato globale nelle tecnologie di termoformatura e saldatura ad alta frequenza per film plastici, materiali a base biologica e fibre naturali. Parte del gruppo Brückner, Kiefel serve produttori di imballaggi, dispositivi medici, frigoriferi e automobili. L'azienda si è espansa nella termoformatura di fibra di cellulosa per applicazioni di imballaggio sostenibili.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- Imballaggi e forniture per la stampa, Forniture medicali e sanitarie, Ricambi e accessori per veicoli
- Markets
- Germania, Stati Uniti, Cina, Giappone, Regno Unito
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