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"Holly" polyetheretherketone lumbar intervertebral fusion - Taiwan Registration e2e8c46efe3d4f83f8cf005baf0dfa1d

Access comprehensive regulatory information for "Holly" polyetheretherketone lumbar 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 e2e8c46efe3d4f83f8cf005baf0dfa1d 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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e2e8c46efe3d4f83f8cf005baf0dfa1d
Registration Details
Taiwan FDA Registration: e2e8c46efe3d4f83f8cf005baf0dfa1d
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Device Details

"Holly" polyetheretherketone lumbar intervertebral fusion
TW: โ€œๅ…จๅˆโ€่š้†š้†š้…ฎ่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

e2e8c46efe3d4f83f8cf005baf0dfa1d

DHY00500268205

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

Apr 14, 2009

Apr 14, 2029