Taiwan FDA registration 707737ff6c6ea641de15b6fe2e8b3af9

"Tecno" multi-item biochemical analysis serum quality control solution (analyzed)

TW: "泰可諾"多項目生化分析血清品管液(已分析)
Taiwan flagTaiwan·Risk Class 2·TECHNO-PATH MANUFACTURING LTD·Registered Jan 11, 2022 – Jan 11, 2027Active
Registration details
Analysis ID
707737ff6c6ea641de15b6fe2e8b3af9
Customs Code
DHA05603520208
Company information
Manufacturer Country
Ireland
Product details
Intended Use
Change Efficacy (Adjusted Text Description) reads: This product can be used as an analyzed quality management serum to monitor the precision of laboratory testing procedures for the analytes listed in this specification.
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 11, 2022
Expiry Date
Jan 11, 2027
About this record

Access comprehensive regulatory information for "Tecno" multi-item biochemical analysis serum quality control solution (analyzed) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 707737ff6c6ea641de15b6fe2e8b3af9 and manufactured by TECHNO-PATH MANUFACTURING LTD. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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