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Knee ONE Intra-articular Injection - Taiwan Registration 755bdfbbb4b21ea095597c2e5f83f9dd

Access comprehensive regulatory information for Knee ONE 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 755bdfbbb4b21ea095597c2e5f83f9dd and manufactured by Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory. The authorized representative in Taiwan is YUNG SHIN PHARM. IND. 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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755bdfbbb4b21ea095597c2e5f83f9dd
Registration Details
Taiwan FDA Registration: 755bdfbbb4b21ea095597c2e5f83f9dd
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Device Details

Knee ONE Intra-articular Injection
TW: ้—œ็›Š ้—œ็ฏ€่…”ๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

755bdfbbb4b21ea095597c2e5f83f9dd

Ministry of Health Medical Device Manufacturing No. 007863

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N0003 Hyaluronic acid implants for the joint cavity

Produced in Taiwan, China

Dates and Status

May 18, 2023

May 18, 2028