Taiwan FDA registration 0fd5cd74590b701e9e5787cd2dc5c3d7

"Tecno" multi-item biochemical analysis urine quality control solution

TW: “泰可諾” 多項目生化分析尿液品管液
Taiwan flagTaiwan·Risk Class 2·TECHNO-PATH MANUFACTURING LTD·Registered Mar 27, 2019 – Mar 27, 2029Active
Registration details
Analysis ID
0fd5cd74590b701e9e5787cd2dc5c3d7
Customs Code
DHA05603238300
Company information
Manufacturer Country
Ireland
Product details
Intended Use
This product can be used as an analytical urine quality control material to monitor the precision of the analytes listed in this leaflet in the laboratory test procedure. Two concentrations of quality control fluid (Concentration 1 and Concentration 2) are supplied in liquid form.
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 urine 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 0fd5cd74590b701e9e5787cd2dc5c3d7 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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