Taiwan FDA registration 08562c0c956e98d45a3a8c29800ca168

"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 Mar 27, 2019 – Mar 27, 2029Active
Registration details
Analysis ID
08562c0c956e98d45a3a8c29800ca168
Customs Code
DHA05603238402
Company information
Manufacturer Country
Ireland
Product details
Intended Use
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
Mar 27, 2019
Expiry Date
Mar 27, 2029
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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 08562c0c956e98d45a3a8c29800ca168 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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