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"Stryker Rebingel" Non-powered Neurosurgical Instruments (Sterile/Unsterilized) - Taiwan Registration 05e1463259bc3fa960fd3ca3fdd3a611

Access comprehensive regulatory information for "Stryker Rebingel" Non-powered Neurosurgical Instruments (Sterile/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 05e1463259bc3fa960fd3ca3fdd3a611 and manufactured by STRYKER LEIBINGER GMBH & CO. KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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05e1463259bc3fa960fd3ca3fdd3a611
Registration Details
Taiwan FDA Registration: 05e1463259bc3fa960fd3ca3fdd3a611
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Device Details

"Stryker Rebingel" Non-powered Neurosurgical Instruments (Sterile/Unsterilized)
TW: "ๅฒ่ณฝๅ…‹ ้›ท่ณ“ๆ ผ็ˆพ" ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘ๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

05e1463259bc3fa960fd3ca3fdd3a611

DHA04400375904

Company Information

Product Details

It is limited to the first level of identification scope of the "Non-powered Neurosurgical Devices (K.4535)" of the Measures for the Classification and Grading of Medical Devices.

K Neuroscience

K.4535 ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ

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Dates and Status

Apr 13, 2006

Apr 13, 2026