Philips Consumer Lifestyle
Dutch innovation in health and everyday consumer products.
Philips is a Dutch multinational producing healthcare technology and consumer lifestyle products including kitchen appliances, personal care devices, and home wellness equipment. The consumer division exports globally through electronics retailers, pharmacy chains, and B2B wholesale partners in both developed and emerging markets. Philips is one of the world's most recognised wholesale consumer brands.
- Type
- Manufacturer
- Location
- Amsterdam, Netherlands
- Founded
- 1891
- Website
- philips.com
- Categories
- Kitchen & Tableware, Medical & Healthcare Supplies, Personal Care
- Markets
- Netherlands, Germany, United States, United Kingdom, China, India, France, Brazil, Australia, Japan
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 2026-08-16 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)