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AVALON Kyphoplasty Kit - Taiwan Registration 065514ded46207ea48def0f54e9ac1e5

Access comprehensive regulatory information for AVALON Kyphoplasty Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 065514ded46207ea48def0f54e9ac1e5 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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065514ded46207ea48def0f54e9ac1e5
Registration Details
Taiwan FDA Registration: 065514ded46207ea48def0f54e9ac1e5
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Device Details

AVALON Kyphoplasty Kit
TW: ้˜ฟๅ‡ก้พ็ƒๅ›ŠๆคŽ้ซ”ๆˆๅž‹่ก“ๅฅ—็ต„
Risk Class 2
MD

Registration Details

065514ded46207ea48def0f54e9ac1e5

Ministry of Health Medical Device Manufacturing No. 005479

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

Produced in Taiwan, China

Dates and Status

Dec 02, 2016

Dec 02, 2026