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“BioTai” Plus Intra-articular Injection - Taiwan Registration 1f5d9b76e68009277e45f9661e96cf4f

Access comprehensive regulatory information for “BioTai” Plus Intra-articular Injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1f5d9b76e68009277e45f9661e96cf4f 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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1f5d9b76e68009277e45f9661e96cf4f
Registration Details
Taiwan FDA Registration: 1f5d9b76e68009277e45f9661e96cf4f
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Device Details

“BioTai” Plus Intra-articular Injection
TW: “博爾泰”關節內注射劑
Risk Class 3
MD
Cancelled

Registration Details

1f5d9b76e68009277e45f9661e96cf4f

Ministry of Health Medical Device Manufacturing No. 005902

Company Information

Taiwan, Province of China

Product Details

N Orthopedic devices

N0003 Hyaluronic acid implants for the joint cavity

Produced in Taiwan, China

Dates and Status

Sep 14, 2017

Aug 22, 2021

Aug 24, 2021

Cancellation Information

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