Tecan
Automatyka laboratoryjna, przyrządy do obsługi cieczy i przyrządy diagnostyczne.
Tecan produkuje urządzenia do automatyzacji laboratoriów, obsługi cieczy i przyrządy diagnostyczne w swoich oddziałach w Männedorf. Firma zaopatruje systemy opieki zdrowotnej, laboratoria, partnerów OEM lub regulowanych klientów eksportowych na swoje notowane na rynkach głównych.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Männedorf, Switzerland
- Founded
- 1980
- Website
- tecan.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną, Maszyny Przemysłowe
- Markets
- Szwajcaria, Stany Zjednoczone, Niemcy, Japonia
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
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- media-mention (green), effective since 2026-07-01 cash.ch
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- places-goods-on-market (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- registered-manufacturer (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- lei-active (green), checked 2026-08-03 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- domain-registered (green), checked 2026-08-03 Domain registry record
- fda-registered (green), checked 2026-08-03 FDA
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality 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)