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“Techno-path”Multichem S Plus (Assayed) - Taiwan Registration 0b8e9e0c8ecdc1b4c0178df4ee301ebe

Access comprehensive regulatory information for “Techno-path”Multichem S Plus (Assayed) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b8e9e0c8ecdc1b4c0178df4ee301ebe and manufactured by TECHNO-PATH MANUFACTURING LTD. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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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0b8e9e0c8ecdc1b4c0178df4ee301ebe
Registration Details
Taiwan FDA Registration: 0b8e9e0c8ecdc1b4c0178df4ee301ebe
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Device Details

“Techno-path”Multichem S Plus (Assayed)
TW: “泰可諾”多項目生化分析血清品管液(已分析)
Risk Class 2
MD
Cancelled

Registration Details

0b8e9e0c8ecdc1b4c0178df4ee301ebe

Ministry of Health Medical Device Import No. 032393

DHA05603239300

Company Information

Product Details

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Apr 02, 2019

Apr 02, 2024

Apr 22, 2022

Cancellation Information

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