Yunnan Baiyao Group Co., Ltd.
Yunnan Baiyao Group es el fabricante de medicina tradicional china más emblemático de China, con sede...
Yunnan Baiyao Group es el fabricante de medicina tradicional china más emblemático de China y tiene su sede en Kunming. El grupo exporta una amplia gama de productos herbarios para la salud, incluidos los renombrados polvos y apósitos Baiyao, líneas para el cuidado del cabello y productos de venta libre para curar heridas. Suministro B2B mayorista disponible para distribuidores de TCM, cadenas de farmacias y minoristas de productos de salud con soporte de registro de productos para los mercados objetivo. Certificado GMP según los estándares NMPA de China. Activo en los mercados de EE. UU., Canadá, Alemania, Australia y Singapur.
- Type
- brand seeking distribution
- Location
- Kunming, China
- Founded
- 1902
- Website
- yunnanbaiyao.com
- Categories
- Suministros médicos y sanitarios, Cuidado y peinado del cabello
- Markets
- Estados Unidos, Alemania, Australia, Singapur, Canadá
Verified facts
- domain-registered (green), checked 2026-08-10 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- debarment-clear (green), checked 2026-08-10 OpenSanctions
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)