Zhejiang Dingtai Pharmaceutical Co., Ltd.
Zhejiang Dingtai Pharmaceutical Co., Ltd. is one of the largest professional production bases of sanitary materials for external use and external application in China. The company has nationally issued pharmaceutical production licenses, medical device production licenses, food production licenses, GMP certificates, ISO14001 certification, ISO9001 certification, CE certification and the World Health Organization supplier certificate issued by the United Nations. The company is a high-tech enterprise in Zhejiang Province and established
Zhejiang Dingtai Pharmaceutical Co., Ltd. is one of the largest professional production bases of sanitary materials for external use and external application in China. The company has nationally issued pharmaceutical production licenses, medical device production licenses, food production licenses, GMP certificates, ISO14001 certification, ISO9001 certification, CE certification and the World Health Organization supplier certificate issued by the United Nations. The company is a high-tech enterprise in Zhejiang Province and has established a provincial-level transdermal preparation research and development center.
- Type
- Manufacturer
- Location
- Tongxiang, China
- Website
- zjdingtai.com
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Pantry & Dry Goods
Listed in a source registry
PLMA Private Label Trade Show 2026 exhibitor directory (Chicago)
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- domain-registered (green), checked 2026-08-10 Domain registry record
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)