Taiwan FDA registration 62452c7d60665d2563faf3b9d6b7d8b6
AlloFuse Plus DBM Paste and Putty
TW: 歐樂芙人體組織骨骼填充物
Taiwan·Risk Class 2·MD·AlloSource·Registered Oct 14, 2016 – Oct 14, 2026ActiveRegistration details
- Analysis ID
- 62452c7d60665d2563faf3b9d6b7d8b6
- License Form
- Ministry of Health Medical Device Import No. 028983
- Customs Code
- DHA05602898306
Company information
- Manufacturer
- AlloSource
- Manufacturer Country
- United States
- Authorized Representative
- LI MIN BIOTECH 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
- Imported from abroad
Dates and status
- Registration Date
- Oct 14, 2016
- Expiry Date
- Oct 14, 2026
About this record
Access comprehensive regulatory information for AlloFuse Plus DBM Paste and Putty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62452c7d60665d2563faf3b9d6b7d8b6 and manufactured by AlloSource. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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