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"Stryker" intervertebral fusion device (sterilization) - Taiwan Registration 452a2bdebb266ad7aa33c17f38d54028

Access comprehensive regulatory information for "Stryker" intervertebral fusion device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 452a2bdebb266ad7aa33c17f38d54028 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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452a2bdebb266ad7aa33c17f38d54028
Registration Details
Taiwan FDA Registration: 452a2bdebb266ad7aa33c17f38d54028
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Device Details

"Stryker" intervertebral fusion device (sterilization)
TW: โ€œๅฒ่ณฝๅ…‹โ€ๆคŽ้–“่žๅˆๅ™จ(ๆป…่Œ)
Risk Class 2

Registration Details

452a2bdebb266ad7aa33c17f38d54028

DHA00602316802

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

Jan 10, 2012

Jan 10, 2027