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Ekang Ketone Liquid (Unsterilized) - Taiwan Registration 8b1e341a0474ed691e25806ff87377dc

Access comprehensive regulatory information for Ekang Ketone Liquid (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b1e341a0474ed691e25806ff87377dc and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is EASY LIFE GREEN TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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8b1e341a0474ed691e25806ff87377dc
Registration Details
Taiwan FDA Registration: 8b1e341a0474ed691e25806ff87377dc
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Device Details

Ekang Ketone Liquid (Unsterilized)
TW: ๆ˜“ๅบท ้…ฎ้ซ”ๅ“็ฎกๆถฒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8b1e341a0474ed691e25806ff87377dc

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)

ๅœ‹็”ข;; ๅง”่จ—่ฃฝ้€ ;; QMS/QSD

Dates and Status

Aug 21, 2019

Aug 21, 2029