Withings SAS
Französischer Hersteller vernetzter Gesundheitsgeräte und intelligenter Waagen.
Withings stellt intelligente Waagen, Hybriduhren, Blutdruckmessgeräte, Schlafsensoren und vernetzte Gesundheitsgeräte her. Das 2008 in Frankreich gegründete Unternehmen beliefert weltweit Kanäle aus den Bereichen Unterhaltungselektronik, Pharmazie, Wellness und Gesundheitswesen.
- Type
- brand seeking distribution
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- Wearables & Personal Devices, Medizin- & Gesundheitsbedarf
- Markets
- Frankreich, Deutschland, Vereinigte Staaten, Vereinigtes Königreich
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)