Taiwan FDA registration 2fa43e1975a4b43fc7b9ceff0e0a4e3e
"Dry" bone plate system
TW: “乾生”骨板系統
Taiwan·Risk Class 2·Dry Biomedical Technology Co., Ltd. Forest Factory·Registered Dec 15, 2009 – Dec 15, 2014CancelledRegistration details
- Analysis ID
- 2fa43e1975a4b43fc7b9ceff0e0a4e3e
- Customs Code
- DHY00500285306
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dry Biomedical Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 15, 2009
- Expiry Date
- Dec 15, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Dry" bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fa43e1975a4b43fc7b9ceff0e0a4e3e and manufactured by Dry Biomedical Technology Co., Ltd. Forest Factory. The authorized representative in Taiwan is Dry Biomedical Technology 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