Taiwan FDA registration fa55b09b549376fad7df0659bf7e0a65
“AlloSource” Puros Demineralized Bone Matrix (DBM)
TW: “亞羅士”普洛斯去礦化骨填充物
Taiwan·Risk Class 2·MD·AlloSource·Registered Jul 26, 2016 – Jul 26, 2026ExpiredRegistration details
- Analysis ID
- fa55b09b549376fad7df0659bf7e0a65
- License Form
- Ministry of Health Medical Device Import No. 028701
- Customs Code
- DHA05602870109
Company information
- Manufacturer
- AlloSource
- Manufacturer Country
- United States
- Authorized Representative
- ZimVie Taiwan 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
- Jul 26, 2016
- Expiry Date
- Jul 26, 2026
About this record
Access comprehensive regulatory information for “AlloSource” Puros Demineralized Bone Matrix (DBM) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa55b09b549376fad7df0659bf7e0a65 and manufactured by AlloSource. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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