Taiwan FDA registration 45b0507b5507186bad429acf879c0d28

Uric acid quality solution (unsterilized)

TW: 暐世尿酸品管液(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered Jul 18, 2022 – Jul 18, 2027Active
Registration details
Analysis ID
45b0507b5507186bad429acf879c0d28
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
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
Input;; QMS/QSD
Dates and status
Registration Date
Jul 18, 2022
Expiry Date
Jul 18, 2027
Companies making similar products

Top companies providing products similar to "Uric acid quality solution (unsterilized)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for Uric acid quality solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 45b0507b5507186bad429acf879c0d28 and manufactured by Hsinchu General Factory of Weishi Biotechnology Co., Ltd. The authorized representative in Taiwan is Hsinchu General Factory of Weishi Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOPTIK TECHNOLOGY, INC., 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations