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"Total" posterior spinal fusion system - Taiwan Registration 133090f2002f3684b97b77d0b9e1615e

Access comprehensive regulatory information for "Total" posterior spinal 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 133090f2002f3684b97b77d0b9e1615e and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER 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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133090f2002f3684b97b77d0b9e1615e
Registration Details
Taiwan FDA Registration: 133090f2002f3684b97b77d0b9e1615e
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Device Details

"Total" posterior spinal fusion system
TW: โ€œๅ…จๅˆโ€่„ŠๆคŽๅพŒๆ–นๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

133090f2002f3684b97b77d0b9e1615e

DHY00500213209

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedics

N.3070 ๆคŽๅผ“่žบ้‡˜็ณป็ตฑ

Domestic

Dates and Status

Feb 16, 2007

Feb 16, 2027