Kiefel GmbH
用于包装、医疗和汽车行业的热成型和焊接机械。
Kiefel GmbH 总部位于巴伐利亚州弗赖拉辛，是塑料薄膜、生物基材料和天然纤维热成型和高频焊接技术领域的全球市场领导者。 Kiefel 隶属于布鲁克纳集团 (Brückner Group)，为包装、医疗设备、冰箱和汽车制造商提供服务。该公司已扩展到可持续包装应用的纤维素纤维热成型领域。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- 包装及印刷用品, 医疗保健用品, 车辆零配件
- Markets
- 德国, 美国, 中国, 日本, 英国
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