"Spite" lumbar fusion device - Taiwan Registration 299c5e61dc9a161db93d51f9a7ed2e48
Access comprehensive regulatory information for "Spite" 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 299c5e61dc9a161db93d51f9a7ed2e48 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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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
Nov 04, 2010
Nov 04, 2020
Jun 07, 2022
Cancellation Information
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