Dätwyler Holding
瑞士精密密封解决方案制造商，为全球制药、医疗器械和工业批发供应链提供关键的橡胶和聚合物组件。
Dätwyler Holding 于 1915 年在瑞士阿尔特多夫成立，是一家全球运营的瑞士工业集团，专门生产由弹性体和聚合物制成的高精度密封解决方案。该公司在五大洲设有 25 个生产工厂，拥有约 8,000 名员工。其医疗保健解决方案部门生产药品瓶盖（药瓶塞、柱塞杆），供应给需要严格符合 GMP 组件的制药制造商和医疗器械批发分销商。密封解决方案部门为汽车、食品和饮料加工以及一般工业批发供应链提供服务。 Dätwyler 的瑞士品质血统和垂直整合的复合能力使其成为关键路径工业采购买家的首选单一来源供应商。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Altdorf, Switzerland
- Founded
- 1915
- Website
- datwyler.com
- Categories
- 工业用品, 工业机械, 医疗保健用品, 橡胶及复合材料产品
- Markets
- 瑞士, 德国, 美国, 法国, 意大利, 荷兰, 英国, 中国, 印度, 巴西
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
- domain-registered (green), checked 2026-08-02 Domain registry record
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)