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
Device Details
Campanile lumbar disc fusion
TW: ๅบท้่
ฐๆคๆค้็ค่ๅๅจ
Risk Class 2

