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AlloFuse Plus DBM Paste and Putty - Taiwan Registration 62452c7d60665d2563faf3b9d6b7d8b6

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..

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.

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62452c7d60665d2563faf3b9d6b7d8b6
Registration Details
Taiwan FDA Registration: 62452c7d60665d2563faf3b9d6b7d8b6
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Device Details

AlloFuse Plus DBM Paste and Putty
TW: ๆญๆจ‚่Š™ไบบ้ซ”็ต„็น”้ชจ้ชผๅกซๅ……็‰ฉ
Risk Class 2
MD

Registration Details

62452c7d60665d2563faf3b9d6b7d8b6

Ministry of Health Medical Device Import No. 028983

DHA05602898306

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

Oct 14, 2016

Oct 14, 2026