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“BioTai” Injectable Bone Void Filler - Taiwan Registration dc990cc5f50bfeba701d5824663cf8e6

Access comprehensive regulatory information for “BioTai” Injectable Bone Void Filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dc990cc5f50bfeba701d5824663cf8e6 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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Registration Details
Taiwan FDA Registration: dc990cc5f50bfeba701d5824663cf8e6
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Device Details

“BioTai” Injectable Bone Void Filler
TW: “博爾泰”注射式骨填充物
Risk Class 3
MD
Cancelled

Registration Details

dc990cc5f50bfeba701d5824663cf8e6

Ministry of Health Medical Device Manufacturing No. 005897

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

Dec 02, 2023

Aug 24, 2021

Cancellation Information

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