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“Techno-path”Multichem S Plus (Unassayed) - Taiwan Registration eafa3521c167a1b469e1fb74b2b84ea5

Access comprehensive regulatory information for “Techno-path”Multichem S Plus (Unassayed) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eafa3521c167a1b469e1fb74b2b84ea5 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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eafa3521c167a1b469e1fb74b2b84ea5
Registration Details
Taiwan FDA Registration: eafa3521c167a1b469e1fb74b2b84ea5
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Device Details

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

Registration Details

eafa3521c167a1b469e1fb74b2b84ea5

Ministry of Health Medical Device Import No. 032392

DHA05603239201

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 01, 2019

Apr 01, 2024

Sep 28, 2022

Cancellation Information

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