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Rhett Gee-ketone Test Tablets (Unsterilized) - Taiwan Registration e4e13c1e8047fa5f0b683d011aef07c0

Access comprehensive regulatory information for Rhett Gee-ketone Test Tablets (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e4e13c1e8047fa5f0b683d011aef07c0 and manufactured by Daqing Factory of Huaguang Biotechnology Co., Ltd. The authorized representative in Taiwan is Daqing Factory of Huaguang Biotechnology Co., Ltd.

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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e4e13c1e8047fa5f0b683d011aef07c0
Registration Details
Taiwan FDA Registration: e4e13c1e8047fa5f0b683d011aef07c0
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Device Details

Rhett Gee-ketone Test Tablets (Unsterilized)
TW: ็‘ž็‰น ๅ‰ๆ˜“้…ฎ้ซ”ๆธฌ่ฉฆ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e4e13c1e8047fa5f0b683d011aef07c0

Company Information

Product Details

Limited to the classification and grading management of medical equipment "Ketone (non-quantitative) test system (A.1435)" first level identification range.

A Clinical chemistry and clinical toxicology

A.1435 Ketone (non-quantitative) testing system

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Sep 21, 2022

Sep 21, 2027