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BeneCheck β-Ketone Test Strip (Non-Sterile) - Taiwan Registration d394a59d96aa94eb42891e8dc2ce7adf

Access comprehensive regulatory information for BeneCheck β-Ketone Test Strip (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d394a59d96aa94eb42891e8dc2ce7adf and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..

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d394a59d96aa94eb42891e8dc2ce7adf
Registration Details
Taiwan FDA Registration: d394a59d96aa94eb42891e8dc2ce7adf
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Device Details

BeneCheck β-Ketone Test Strip (Non-Sterile)
TW: 百捷 酮體試片 (未滅菌)
Risk Class 1
MD

Registration Details

d394a59d96aa94eb42891e8dc2ce7adf

Ministry of Health Medical Device Manufacturing No. 008611

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1435 Ketone (non-quantitative) test system

Produced in Taiwan, China

Dates and Status

Sep 23, 2020

Sep 23, 2025