Withings SAS
Nhà sản xuất thiết bị y tế kết nối và cân thông minh của Pháp.
Withings sản xuất cân thông minh, đồng hồ lai, máy đo huyết áp, cảm biến giấc ngủ và các thiết bị y tế được kết nối. Được thành lập tại Pháp vào năm 2008, công ty cung cấp các kênh điện tử tiêu dùng, dược phẩm, sức khỏe và chăm sóc sức khỏe trên toàn thế giới.
- Type
- brand seeking distribution
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- Thiết bị đeo và thiết bị cá nhân, Vật tư y tế và chăm sóc sức khỏe
- Markets
- Pháp, Đức, Hoa Kỳ, Vương quốc Anh
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)