"Spite" Romeo lumbar posterior fusion system - Taiwan Registration 6d5719d8ab5805c2b9084d7116a0ceec
Access comprehensive regulatory information for "Spite" Romeo lumbar posterior fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d5719d8ab5805c2b9084d7116a0ceec 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.3070 ๆคๅผ่บ้็ณป็ตฑ
import
Dates and Status
Sep 15, 2010
Sep 15, 2020
Jun 07, 2022
Cancellation Information
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