Taiwan FDA registration 99a16c7b0437711d9c5f3a48a93b8dd2

Glucose Tube Solution (Unsterilized)

TW: 暐世葡萄糖品管液 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered Jul 27, 2022 – Jul 27, 2027Active
Registration details
Analysis ID
99a16c7b0437711d9c5f3a48a93b8dd2
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
國產;; QMS/QSD
Dates and status
Registration Date
Jul 27, 2022
Expiry Date
Jul 27, 2027
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About this record

Access comprehensive regulatory information for Glucose Tube 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 99a16c7b0437711d9c5f3a48a93b8dd2 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, 4 companies making similar products including BIOPTIK TECHNOLOGY, INC., Qinli Biotechnology Co., Ltd. new tree factory, and 5 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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