Dätwyler Holding
Produsen solusi penyegelan presisi Swiss yang memasok komponen karet dan polimer penting ke farmasi, perangkat medis, dan rantai pasokan grosir industri di seluruh dunia.
Dätwyler Holding, didirikan di Altdorf, Swiss pada tahun 1915, adalah grup industri Swiss yang beroperasi secara global dan berspesialisasi dalam solusi penyegelan presisi tinggi yang terbuat dari elastomer dan polimer. Perusahaan ini mempekerjakan sekitar 8.000 orang di 25 fasilitas produksi di lima benua. Divisi Solusi Layanan Kesehatannya memproduksi penutup farmasi (penutup botol, batang pendorong) yang dipasok ke produsen farmasi dan distributor grosir perangkat medis yang memerlukan komponen ketat yang sesuai dengan GMP. Divisi Sealing Solutions melayani otomotif, pemrosesan makanan dan minuman, serta rantai pasokan grosir industri umum. Silsilah Dätwyler yang berkualitas di Swiss dan kemampuan penggabungan yang terintegrasi secara vertikal menjadikannya pemasok sumber tunggal pilihan bagi pembeli pengadaan industri jalur kritis.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Altdorf, Switzerland
- Founded
- 1915
- Website
- datwyler.com
- Categories
- Perlengkapan Industri, Mesin Industri, Perlengkapan Medis & Kesehatan, Produk Karet & Komposit
- Markets
- Swiss, Jerman, Amerika Serikat, Prancis, Italia, Belanda, Inggris Raya, Tiongkok, India, Brasil
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)