Yunnan Baiyao Group Co., Ltd.
Yunnan Baiyao Group , самый знаковый производитель традиционной китайской медицины в Китае, штаб-квартира…
Yunnan Baiyao Group , самый известный производитель традиционной китайской медицины в Китае со штаб-квартирой в Куньмине. Группа экспортирует широкий спектр продуктов для здоровья на основе трав, включая знаменитый порошок и пластыри Baiyao, линии по уходу за волосами и безрецептурные средства для заживления ран. Оптовые поставки B2B доступны для дистрибьюторов TCM, аптечных сетей и розничных продавцов товаров медицинского назначения с поддержкой регистрации продукта на целевых рынках. GMP сертифицирован по китайским стандартам NMPA. Активен на рынках США, Канады, Германии, Австралии и Сингапура.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kunming, China
- Founded
- 1902
- Website
- yunnanbaiyao.com
- Categories
- Медицинские товары и расходники, Уход и укладка волос
- Markets
- Соединенные Штаты, Германия, Австралия, Сингапур, Канада
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
- 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 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-10 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- 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)