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"Leif" spine surgery manual instruments (unsterilized) - Taiwan Registration b77820da3601d1d05c85a52b3e40cb53

Access comprehensive regulatory information for "Leif" spine surgery manual instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b77820da3601d1d05c85a52b3e40cb53 and manufactured by LIFE INSTRUMENTS CORPORATION. The authorized representative in Taiwan is U-CHANTER ENTERPRISE 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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b77820da3601d1d05c85a52b3e40cb53
Registration Details
Taiwan FDA Registration: b77820da3601d1d05c85a52b3e40cb53
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Device Details

"Leif" spine surgery manual instruments (unsterilized)
TW: โ€œ่Šๅคซโ€่„ŠๆคŽๆ‰‹่ก“ๆ‰‹ๅ‹•ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b77820da3601d1d05c85a52b3e40cb53

DHA04400585803

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".

K Neuroscience

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

import

Dates and Status

May 16, 2007

May 16, 2012

Apr 16, 2014

Cancellation Information

Logged out

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