Philips Consumer Lifestyle
Innovación holandesa en salud y productos de consumo cotidiano.
Philips es una multinacional holandesa que produce tecnología sanitaria y productos de estilo de vida para el consumidor, incluidos electrodomésticos de cocina, dispositivos de cuidado personal y equipos de bienestar para el hogar. La división de consumo exporta a nivel mundial a través de minoristas de productos electrónicos, cadenas de farmacias y socios mayoristas B2B en mercados desarrollados y emergentes. Philips es una de las marcas de consumo mayorista más reconocidas del mundo.
- Type
- brand seeking distribution
- Location
- Amsterdam, Netherlands
- Founded
- 1891
- Website
- philips.com
- Categories
- Cocina y menaje, Suministros médicos y sanitarios, Cuidado personal
- Markets
- Países Bajos, Alemania, Estados Unidos, Reino Unido, China, India, Francia, Brasil, Australia, Japón
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- fda-registered (green), checked 2026-08-09 FDA
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- 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
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- Good Manufacturing Practice
- 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)