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"Smysmith" Spinal posterior fixation system - Taiwan Registration bc35cb22f26edbfa6468b66d6d6152e9

Access comprehensive regulatory information for "Smysmith" Spinal posterior fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc35cb22f26edbfa6468b66d6d6152e9 and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia 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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bc35cb22f26edbfa6468b66d6d6152e9
Registration Details
Taiwan FDA Registration: bc35cb22f26edbfa6468b66d6d6152e9
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Device Details

"Smysmith" Spinal posterior fixation system
TW: โ€œๅฒ้บฅๅฏ†ๆ–ฏโ€ ่„ŠๆคŽๅพŒๆ–นๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

bc35cb22f26edbfa6468b66d6d6152e9

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

Sep 22, 2017

Sep 22, 2027