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"Holly" PEEK intervertebral stent system - Taiwan Registration fabe564398dfb1aa22c6ddfcf10a09bf

Access comprehensive regulatory information for "Holly" PEEK intervertebral stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fabe564398dfb1aa22c6ddfcf10a09bf 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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fabe564398dfb1aa22c6ddfcf10a09bf
Registration Details
Taiwan FDA Registration: fabe564398dfb1aa22c6ddfcf10a09bf
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Device Details

"Holly" PEEK intervertebral stent system
TW: โ€œๅ…จๅˆโ€่š้†š้†š้…ฎๆคŽ้–“ๆ”ฏๆžถ็ณป็ตฑ
Risk Class 2

Registration Details

fabe564398dfb1aa22c6ddfcf10a09bf

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

Domestic

Dates and Status

Aug 20, 2012

Aug 20, 2027