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"Stryker" lumbar fusion device - Taiwan Registration e270cbd02375f2f7b6d31fe5f09ee826

Access comprehensive regulatory information for "Stryker" lumbar fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e270cbd02375f2f7b6d31fe5f09ee826 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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e270cbd02375f2f7b6d31fe5f09ee826
Registration Details
Taiwan FDA Registration: e270cbd02375f2f7b6d31fe5f09ee826
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Device Details

"Stryker" lumbar fusion device
TW: โ€œๅฒ่ณฝๅ…‹โ€่…ฐๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

e270cbd02375f2f7b6d31fe5f09ee826

DHA00602257303

Company Information

France

Product Details

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

N Orthopedics

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

import

Dates and Status

Jun 30, 2011

Jun 30, 2026