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"Stryker" side-open lumbar fusion device (sterilization) - Taiwan Registration 545fe4e01361d901984909a517fdc755

Access comprehensive regulatory information for "Stryker" side-open lumbar 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 545fe4e01361d901984909a517fdc755 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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545fe4e01361d901984909a517fdc755
Registration Details
Taiwan FDA Registration: 545fe4e01361d901984909a517fdc755
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Device Details

"Stryker" side-open lumbar fusion device (sterilization)
TW: โ€œๅฒ่ณฝๅ…‹โ€ๅด้–‹่…ฐๆคŽ้–“่žๅˆๅ™จ(ๆป…่Œ)
Risk Class 2

Registration Details

545fe4e01361d901984909a517fdc755

DHA00602338507

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

Mar 22, 2012

Mar 22, 2027