Taiwan FDA registration f0dc31ebaeee8f64ca50dd8bf66fdeb5
“AlloSource” AlloFuse DBM
TW: “歐樂”歐樂芙去礦化異體植骨
Taiwan·Risk Class 2·MD·AlloSource·Registered Mar 17, 2016 – Mar 17, 2026ExpiredRegistration details
- Analysis ID
- f0dc31ebaeee8f64ca50dd8bf66fdeb5
- License Form
- Ministry of Health Medical Device Import No. 028333
- Customs Code
- DHA05602833306
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
- Mar 17, 2016
- Expiry Date
- Mar 17, 2026
About this record
Access comprehensive regulatory information for “AlloSource” AlloFuse DBM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0dc31ebaeee8f64ca50dd8bf66fdeb5 and manufactured by AlloSource. The authorized representative in Taiwan is LI MIN BIOTECH 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