Taiwan FDA registration 235efaf1d6b8dfd8fdb32c069e1b2512

Glucose Tube Solution (Unsterilized)

TW: 易美測 葡萄糖品管液 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·BIOPTIK TECHNOLOGY, INC.·Registered Apr 18, 2008 – Apr 18, 2028Active
Registration details
Analysis ID
235efaf1d6b8dfd8fdb32c069e1b2512
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
BIOPTIK TECHNOLOGY, INC.
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
Domestic
Dates and status
Registration Date
Apr 18, 2008
Expiry Date
Apr 18, 2028
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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 235efaf1d6b8dfd8fdb32c069e1b2512 and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Qinli Biotechnology Co., Ltd. new tree factory, APEX BIOTECHNOLOGY CORPORATION, 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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