Taiwan FDA registration 394f4a5eb1129ac011b632c35eca31d0

Inorganic phosphorus reagent set (unsterilized)

TW: 〝朕江〞無機磷試劑套組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Apr 25, 2022 – Apr 25, 2027Active
Registration details
Analysis ID
394f4a5eb1129ac011b632c35eca31d0
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LANNER BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, phosphoric acid (inorganic) test system (A.1580) first level identification range.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1580 Phosphoric acid (inorganic) test system
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Apr 25, 2022
Expiry Date
Apr 25, 2027
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About this record

Access comprehensive regulatory information for Inorganic phosphorus reagent set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 394f4a5eb1129ac011b632c35eca31d0 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., 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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