Withings SAS
Французский производитель подключенных медицинских устройств и умных весов.
Withings производит умные весы, гибридные часы, тонометры, датчики сна и подключенные устройства для здоровья. Основанная во Франции в 2008 году, компания поставляет бытовую электронику, фармацевтику, товары для здоровья и здравоохранения по всему миру.
- Type
- brand seeking distribution
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- Носимые устройства, Медицинские товары и расходники
- Markets
- Франция, Германия, Соединенные Штаты, Великобритания
Verified facts
- registry-activity (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- domain-registered (green), checked 2026-08-26 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- financials-published (green), checked 2023-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-active-global (green), checked 2026-08-07 INSEE SIRENE (Registre national des entreprises)
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- listed-in-registry (green), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- registry-id-verified (green), checked 2026-06-04 Annuaire des Entreprises (INSEE / INPI)
Claimed certifications
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)