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“AlloSource” AlloFuse DBM - Taiwan Registration f0dc31ebaeee8f64ca50dd8bf66fdeb5

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..

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f0dc31ebaeee8f64ca50dd8bf66fdeb5
Registration Details
Taiwan FDA Registration: f0dc31ebaeee8f64ca50dd8bf66fdeb5
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Device Details

“AlloSource” AlloFuse DBM
TW: “歐樂”歐樂芙去礦化異體植骨
Risk Class 2
MD

Registration Details

f0dc31ebaeee8f64ca50dd8bf66fdeb5

Ministry of Health Medical Device Import No. 028333

DHA05602833306

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

Mar 17, 2016

Mar 17, 2026