Taiwan FDA registration f666b677755a0166421ab573472ccc79

"Tecno" multi-item biochemical analysis quality control solution

TW: “泰可諾” 多項目生化分析品管液
Taiwan flagTaiwan·Risk Class 2·TECHNO-PATH MANUFACTURING LTD·Registered Feb 12, 2015 – Feb 12, 2030Active
Registration details
Analysis ID
f666b677755a0166421ab573472ccc79
Customs Code
DHA05602707202
Company information
Manufacturer Country
Ireland
Product details
Intended Use
The performance change is that this product can be used as a single concentration of analyzed quality control material to monitor the precision of the analytes listed in this manual during laboratory test procedures.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1660 Quality control materials (analytical and non-analytical)
Import Information
import
Dates and status
Registration Date
Feb 12, 2015
Expiry Date
Feb 12, 2030
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About this record

Access comprehensive regulatory information for "Tecno" multi-item biochemical analysis quality control solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f666b677755a0166421ab573472ccc79 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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