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Campanile cervical disc fusion - Taiwan Registration 383f80946e110c44ef609300b0f71822

Access comprehensive regulatory information for Campanile cervical disc fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 383f80946e110c44ef609300b0f71822 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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383f80946e110c44ef609300b0f71822
Registration Details
Taiwan FDA Registration: 383f80946e110c44ef609300b0f71822
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Device Details

Campanile cervical disc fusion
TW: ๅบท้‰‘้ ธๆคŽๆคŽ้–“็›ค่žๅˆๅ™จ
Risk Class 2

Registration Details

383f80946e110c44ef609300b0f71822

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

May 04, 2013

May 04, 2028