Withings SAS
Produsen perangkat kesehatan dan skala pintar yang terhubung dari Perancis.
Withings memproduksi timbangan pintar, jam tangan hybrid, monitor tekanan darah, sensor tidur, dan perangkat kesehatan yang terhubung. Didirikan di Perancis pada tahun 2008, perusahaan ini memasok saluran elektronik konsumen, farmasi, kesehatan, dan perawatan kesehatan di seluruh dunia.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- Perangkat yang Dapat Dipakai & Perangkat Pribadi, Perlengkapan Medis & Kesehatan
- Markets
- Prancis, Jerman, Amerika Serikat, Inggris Raya
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
- registry-activity (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- directors-on-file (green), checked 2026-09-18 INSEE Sirene (annuaire-entreprises)
- 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 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- financials-published (green), effective since 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 (amber), 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), effective since 2026-06-04 Annuaire des Entreprises (INSEE / INPI)
Claimed certifications, not confirmed by us
- 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)