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“BioTai” Bone Graft Substitute - Taiwan Registration 69137df093e366e8f703bca0b1ff74a2

Access comprehensive regulatory information for “BioTai” Bone Graft Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69137df093e366e8f703bca0b1ff74a2 and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..

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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69137df093e366e8f703bca0b1ff74a2
Registration Details
Taiwan FDA Registration: 69137df093e366e8f703bca0b1ff74a2
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Device Details

“BioTai” Bone Graft Substitute
TW: “博爾泰”人工骨粉
Risk Class 2
MD
Cancelled

Registration Details

69137df093e366e8f703bca0b1ff74a2

Ministry of Health Medical Device Manufacturing No. 005899

Company Information

Taiwan, Province of China

Product Details

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Produced in Taiwan, China

Dates and Status

Sep 04, 2017

Nov 05, 2019

Aug 24, 2021

Cancellation Information

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