Medela
Tire-lait, produits de soins néonatals et systèmes d'aspiration médicale.
Medela fabrique des tire-lait, des produits de soins néonatals et des systèmes d'aspiration médicale depuis sa base de Baar. La société fournit des clients de détail, de gros, industriels et d'exportation sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Baar, Switzerland
- Founded
- 1961
- Website
- medela.com
- Categories
- Fournitures médicales et de santé, Soin et alimentation de bébé
- Markets
- Suisse, États-Unis, Allemagne, Japon
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- 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-lapsed (amber), checked 2026-08-30 GLEIF global LEI register (golden copy)
- operating-permit (green), checked 2023-12-01 SHAB, Swiss Official Gazette of Commerce
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
- fda-registered (green), checked 2026-07-21 FDA
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)