Taiwan FDA registration 7046b15a852b6346db64a9ae62b87e9a
“BoniPlus” Bone Graft
TW: “寶凝加”骨填補物
Taiwan·Risk Class 2·MD·Heyi Technology Co., Ltd. Precision Factory·Registered Feb 07, 2018 – Feb 07, 2028ActiveRegistration details
- Analysis ID
- 7046b15a852b6346db64a9ae62b87e9a
- License Form
- Ministry of Health Medical Device Manufacturing No. 006022
Company information
- Manufacturer
- Heyi Technology Co., Ltd. Precision Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MONTJADE ENGINEERING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 07, 2018
- Expiry Date
- Feb 07, 2028
About this record
Access comprehensive regulatory information for “BoniPlus” Bone Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7046b15a852b6346db64a9ae62b87e9a and manufactured by Heyi Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is MONTJADE ENGINEERING 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