Dätwyler Holding
Swiss precision sealing solutions manufacturer supplying critical rubber and polymer components to pharma, medical device, and industrial wholesale supply chains worldwide.
Dätwyler Holding, founded in Altdorf, Switzerland in 1915, is a globally operating Swiss industrial group specializing in high-precision sealing solutions made from elastomers and polymers. The company employs approximately 8,000 people across 25 production facilities on five continents. Its Healthcare Solutions division manufactures pharmaceutical closures (vial stoppers, plunger rods) supplied to pharma manufacturers and medical device wholesale distributors requiring stringent GMP-compliant components. The Sealing Solutions division serves automotive, food-and-beverage processing, and general industrial wholesale supply chains. Dätwyler's Swiss quality pedigree and vertically integrated compounding capability make it a preferred single-source supplier for critical-path industrial procurement buyers.
- Type
- Manufacturer
- Location
- Altdorf, Switzerland
- Founded
- 1915
- Website
- datwyler.com
- Categories
- Industrial Supplies, Industrial Machinery, Medical & Healthcare Supplies, Rubber & Composite Products
- Markets
- Switzerland, Germany, United States, France, Italy, Netherlands, United Kingdom, China, India, Brazil
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
Claimed certifications
- 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)