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Lightning Polymer Composite Material Intervertebral Fusion - Taiwan Registration a9bfdfcc535ab496c886decc0e81937b

Access comprehensive regulatory information for Lightning Polymer Composite Material Intervertebral Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9bfdfcc535ab496c886decc0e81937b 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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a9bfdfcc535ab496c886decc0e81937b
Registration Details
Taiwan FDA Registration: a9bfdfcc535ab496c886decc0e81937b
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Device Details

Lightning Polymer Composite Material Intervertebral Fusion
TW: ้›ท็‰นไฝณ้ซ˜ๅˆ†ๅญ่ค‡ๅˆๆๆ–™ๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

a9bfdfcc535ab496c886decc0e81937b

DHY00500309100

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

Domestic

Dates and Status

Sep 07, 2010

Sep 07, 2025