Taiwan FDA registration c0ec487460153959664a00ef76bcfe8f

Ficon Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized)

TW: "飛確" 呼吸道融合細胞病毒快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·Baoling Fujin Biotechnology Co., Ltd. Xizhi Plant No. 2 Factory·Registered Dec 09, 2015 – Dec 09, 2025Expired

Registration details

Analysis ID: c0ec487460153959664a00ef76bcfe8f

Company information

Manufacturer: Baoling Fujin Biotechnology Co., Ltd. Xizhi Plant No. 2 Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PANION & BF BIOTECH INC.

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3480 呼吸道融合細胞病毒血清試劑
Import Information: Domestic

Dates and status

Registration Date: Dec 09, 2015
Expiry Date: Dec 09, 2025

About this record

Access comprehensive regulatory information for Ficon Respiratory Fusion Cell Virus 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 c0ec487460153959664a00ef76bcfe8f and manufactured by Baoling Fujin Biotechnology Co., Ltd. Xizhi Plant No. 2 Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..

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