Taiwan FDA registration 6fbe1852579d6e49475c124ab2dc0630

"TIB" Olfactory test device (Non-Sterile)

TW: "牛耳" 嗅覺測試裝置 (未滅菌)

Taiwan·Risk Class 1·MD·Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory·Registered Nov 23, 2018 – Nov 23, 2023Expired

Registration details

Analysis ID: 6fbe1852579d6e49475c124ab2dc0630
License Form: Ministry of Health Medical Device Manufacturing No. 007538

Company information

Manufacturer: Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Niuer International Biotechnology Co., Ltd

Product details

Intended Use: Limited to the first level identification range of the "olfactory test device (G.1600)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): G ENT device
Product Type (Level 2): G1600 olfactory test device
Import Information: Produced in Taiwan, China; Contract manufacturing

Dates and status

Registration Date: Nov 23, 2018
Expiry Date: Nov 23, 2023

About this record

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.

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