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BIOMOLD Synthetic Bone Graft - Taiwan Registration ee6cf33071b91cc7c2a4d6a4f1c9f574

Access comprehensive regulatory information for BIOMOLD Synthetic Bone Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee6cf33071b91cc7c2a4d6a4f1c9f574 and manufactured by İDEA İLAÇ ÜRETİM SANAYİ LTD. ŞTİ. The authorized representative in Taiwan is XELITE BIOMED 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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ee6cf33071b91cc7c2a4d6a4f1c9f574
Registration Details
Taiwan FDA Registration: ee6cf33071b91cc7c2a4d6a4f1c9f574
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Device Details

BIOMOLD Synthetic Bone Graft
TW: 拜莫特生物可吸收補骨物
Risk Class 2
MD

Registration Details

ee6cf33071b91cc7c2a4d6a4f1c9f574

Ministry of Health Medical Device Import No. 035576

DHA05603557600

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3045 Absorbable calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Jun 10, 2022

Jun 10, 2027