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"Spite" Romeo posterior lumbar fusion system - Taiwan Registration 238f60cfe7cdb0de774d755cf67d4c19

Access comprehensive regulatory information for "Spite" Romeo posterior lumbar 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 238f60cfe7cdb0de774d755cf67d4c19 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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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238f60cfe7cdb0de774d755cf67d4c19
Registration Details
Taiwan FDA Registration: 238f60cfe7cdb0de774d755cf67d4c19
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Device Details

"Spite" Romeo posterior lumbar fusion system
TW: โ€œๅธไฝฐ็‰นโ€็พ…ๅฏ†ๆญ่…ฐๆคŽๅพŒ่ทฏ่žๅˆ็ณป็ตฑ
Risk Class 2

Registration Details

238f60cfe7cdb0de774d755cf67d4c19

DHA00602313602

Company Information

Switzerland

Product Details

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

N Orthopedics

N.3070 ๆคŽๅผ“่žบ้‡˜็ณป็ตฑ

import

Dates and Status

Dec 22, 2011

Dec 22, 2026