Kiefel GmbH
포장, 의료 및 자동차 부문을 위한 열성형 및 용접 기계.
바이에른주 프레일라싱(Freilassing)에 본사를 둔 Kiefel GmbH는 플라스틱 필름, 바이오 기반 소재 및 천연 섬유용 열성형 및 고주파 용접 기술 분야의 글로벌 시장 리더입니다. Brückner Group의 일부인 Kiefel은 포장, 의료 기기, 냉장고 및 자동차 제조업체에 서비스를 제공합니다. 이 회사는 지속 가능한 포장 응용 분야를 위해 셀룰로오스 섬유 열성형 분야로 사업을 확장했습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Freilassing, Germany
- Founded
- 1945
- Website
- kiefel.com
- Categories
- 포장 및 인쇄 용품, 의료 및 건강 관리 용품, 차량 부품 및 액세서리
- Markets
- 독일, 미국, 중국, 일본, 영국
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