"Adir" posterior lumbar fusion device - Taiwan Registration 9225678dee85099cb3ba71cdb0ee3ee4
Access comprehensive regulatory information for "Adir" posterior lumbar fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9225678dee85099cb3ba71cdb0ee3ee4 and manufactured by LDR Medical. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..
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Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedics
N.3060 ๆค้ซ้ไน่ๆค็ฏๆญฃๅบๅฎ็ฉ
import
Dates and Status
Jul 06, 2013
Jul 06, 2018
Jun 07, 2022
Cancellation Information
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