Taiwan FDA registration 88b92b8b2ee1a25123e0ef2edcd732b4
Sulodine HBE
TW: 速樂定HBE
Registration details
- Analysis ID
- 88b92b8b2ee1a25123e0ef2edcd732b4
- Customs Code
- DHY00500146801
Company information
- Manufacturer
- Dayuan Factory of Taifu Pharmaceutical Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Unit
- TEST/KIT
Dates and status
- Registration Date
- Jul 01, 2005
- Expiry Date
- Oct 29, 2006
- Cancellation Date
- Oct 15, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Sulodine HBE in Taiwan's medical device market through Pure Global AI's free database. is registered under number 88b92b8b2ee1a25123e0ef2edcd732b4 and manufactured by Dayuan Factory of Taifu Pharmaceutical Co., Ltd. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices