Taiwan FDA registration 2eb0cf736522673a99d2698ce7df13c1

Fiquor A+B Influenza Rapid Test Reagent (Unsterilized)

TW: "飛確" A+B型流行性感冒快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory·Registered Oct 29, 2015 – Oct 29, 2020Cancelled

Registration details

Analysis ID: 2eb0cf736522673a99d2698ce7df13c1

Company information

Manufacturer: Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PANION & BF BIOTECH INC.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3330 流感病毒血清試劑
Import Information: Domestic

Dates and status

Registration Date: Oct 29, 2015
Expiry Date: Oct 29, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Fiquor A+B Influenza Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2eb0cf736522673a99d2698ce7df13c1 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..

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