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"Hormedeka" manual replacement combination system - Taiwan Registration 95a3abb93aa2ce47f2d2d7e937e901cb

Access comprehensive regulatory information for "Hormedeka" manual replacement combination system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 95a3abb93aa2ce47f2d2d7e937e901cb and manufactured by HOWMEDICA INTERNATIONAL S. DE R.L.. 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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95a3abb93aa2ce47f2d2d7e937e901cb
Registration Details
Taiwan FDA Registration: 95a3abb93aa2ce47f2d2d7e937e901cb
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Device Details

"Hormedeka" manual replacement combination system
TW: "ๅฅฝ็พŽๅพ—ๅก" ไบบๅทฅๆ›ฟๆ›็‰ฉ็ต„ๅˆ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

95a3abb93aa2ce47f2d2d7e937e901cb

DHA00600933905

Company Information

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Nov 19, 1999

Apr 16, 2023

Dec 08, 2022

Cancellation Information

Logged out

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