Taiwan FDA registration e0b68ab5002101b9f0bb0b060d7dd006

“Techno-path” Multichem WBT

TW: “泰可諾” 多項目分析全血品管液
Taiwan flagTaiwan·Risk Class 2·MD·TECHNO-PATH MANUFACTURING LTD·Registered Jul 01, 2020 – Jul 01, 2025Expired
Registration details
Analysis ID
e0b68ab5002101b9f0bb0b060d7dd006
License Form
Ministry of Health Medical Device Import No. 033499
Customs Code
DHA05603349908
Company information
Manufacturer Country
Ireland
Product details
Intended Use
This product can be used as an analytical quality management material to monitor the precision of the analytes listed in this imitation list in laboratory test procedures. This product contains 3 different concentrations of quality control solutions, prepared with human whole blood.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 01, 2020
Expiry Date
Jul 01, 2025
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About this record

Access comprehensive regulatory information for “Techno-path” Multichem WBT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0b68ab5002101b9f0bb0b060d7dd006 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, 1 companies making similar products including TECHNO-PATH MANUFACTURING LTD, and 1 recent registrations in the same category. 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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