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Glucose Tube Solution (Unsterilized) - Taiwan Registration 235efaf1d6b8dfd8fdb32c069e1b2512

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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235efaf1d6b8dfd8fdb32c069e1b2512
Registration Details
Taiwan FDA Registration: 235efaf1d6b8dfd8fdb32c069e1b2512
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Device Details

Glucose Tube Solution (Unsterilized)
TW: ๆ˜“็พŽๆธฌ ่‘ก่„็ณ–ๅ“็ฎกๆถฒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

235efaf1d6b8dfd8fdb32c069e1b2512

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

Domestic

Dates and Status

Apr 18, 2008

Apr 18, 2028