Medela
Молокоотсосы, средства ухода за новорожденными и медицинские аспираторы.
Medela производит молокоотсосы, средства ухода за новорожденными и медицинские аспирационные системы на своей базе в Бааре. Компания снабжает розничных, оптовых, промышленных и экспортных клиентов на своих перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Baar, Switzerland
- Founded
- 1961
- Website
- medela.com
- Categories
- Медицинские товары и расходники, Уход и кормление малышей
- Markets
- Швейцария, Соединенные Штаты, Германия, Япония
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)