Pure Global

“Techno-path”Multichem IA Plus - Taiwan Registration 42262afed213d9529c2a66c0d0bb69ee

Access comprehensive regulatory information for “Techno-path”Multichem IA Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42262afed213d9529c2a66c0d0bb69ee 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
42262afed213d9529c2a66c0d0bb69ee
Registration Details
Taiwan FDA Registration: 42262afed213d9529c2a66c0d0bb69ee
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Techno-path”Multichem IA Plus
TW: “泰可諾” 多項目免疫分析品管液
Risk Class 2
MD

Registration Details

42262afed213d9529c2a66c0d0bb69ee

Ministry of Health Medical Device Import No. 032430

DHA05603243006

Company Information

Product Details

This product can be used as an analysed mass management serum to monitor the precision of laboratory testing procedures for the analytes listed in this specification.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

May 10, 2019

May 10, 2024