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Campanile lumbar disc fusion - Taiwan Registration 2f638fa2a3679ed7de4d7dba9683dbe8

Access comprehensive regulatory information for Campanile lumbar disc fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f638fa2a3679ed7de4d7dba9683dbe8 and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia 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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2f638fa2a3679ed7de4d7dba9683dbe8
Registration Details
Taiwan FDA Registration: 2f638fa2a3679ed7de4d7dba9683dbe8
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Device Details

Campanile lumbar disc fusion
TW: ๅบท้‰‘่…ฐๆคŽๆคŽ้–“็›ค่žๅˆๅ™จ
Risk Class 2

Registration Details

2f638fa2a3679ed7de4d7dba9683dbe8

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

Domestic

Dates and Status

Dec 18, 2012

Dec 18, 2027