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"TIB" Olfactory test device (Non-Sterile) - Taiwan Registration 6fbe1852579d6e49475c124ab2dc0630

Access comprehensive regulatory information for "TIB" Olfactory test device (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 6fbe1852579d6e49475c124ab2dc0630 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory. The authorized representative in Taiwan is Niuer International 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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6fbe1852579d6e49475c124ab2dc0630
Registration Details
Taiwan FDA Registration: 6fbe1852579d6e49475c124ab2dc0630
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Device Details

"TIB" Olfactory test device (Non-Sterile)
TW: "็‰›่€ณ" ๅ—…่ฆบๆธฌ่ฉฆ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6fbe1852579d6e49475c124ab2dc0630

Ministry of Health Medical Device Manufacturing No. 007538

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "olfactory test device (G.1600)" of the Measures for the Administration of Medical Devices.

G ENT device

G1600 olfactory test device

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Nov 23, 2018

Nov 23, 2023