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“AlloSource” Puros Demineralized Bone Matrix (DBM) - Taiwan Registration fa55b09b549376fad7df0659bf7e0a65

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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fa55b09b549376fad7df0659bf7e0a65
Registration Details
Taiwan FDA Registration: fa55b09b549376fad7df0659bf7e0a65
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Device Details

“AlloSource” Puros Demineralized Bone Matrix (DBM)
TW: “亞羅士”普洛斯去礦化骨填充物
Risk Class 2
MD

Registration Details

fa55b09b549376fad7df0659bf7e0a65

Ministry of Health Medical Device Import No. 028701

DHA05602870109

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Jul 26, 2016

Jul 26, 2026