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"Clariance" Orthopedic manual surgical instrument (Non-Sterile) - Taiwan Registration 37ba2dddd1d2ba74f1997ca5b3248148

Access comprehensive regulatory information for "Clariance" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 37ba2dddd1d2ba74f1997ca5b3248148 and manufactured by CLARIANCE. The authorized representative in Taiwan is LI MIN BIOTECH 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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37ba2dddd1d2ba74f1997ca5b3248148
Registration Details
Taiwan FDA Registration: 37ba2dddd1d2ba74f1997ca5b3248148
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Device Details

"Clariance" Orthopedic manual surgical instrument (Non-Sterile)
TW: "ๅ…‹่Šๅ…’" ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

37ba2dddd1d2ba74f1997ca5b3248148

Ministry of Health Medical Device Import No. 014802

DHA09401480209

Company Information

France

Product Details

N Orthopedic devices

N4540 Manual osteologic surgery instrument

Imported from abroad

Dates and Status

Dec 29, 2014

Dec 29, 2019

Jun 22, 2022

Cancellation Information

Logged out

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