Taiwan FDA registration 0c1795622d8796426ffa2e4f4ff97dde

Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell Virus (Unsterilized)

TW: “生研”快納威流行性感冒暨呼吸道融合細胞病毒快速檢驗套組 (未滅菌)

Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered May 15, 2014 – May 15, 2024Expired

Registration details

Analysis ID: 0c1795622d8796426ffa2e4f4ff97dde
Customs Code: DHA09401414308

Company information

Manufacturer: DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
Manufacturer Country: Japan
Authorized Representative: TUNYEN ENTERPRISE CORPORATION

Product details

Intended Use: It is limited to the first-level identification scope of the "Respiratory Fusion Cell Virus Serum Reagent (C.3480)" and "Influenza Virus Serum Reagent (C.3330)" of the Classification and Grading Management Measures for Medical Devices.
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;; C.3330 流感病毒血清試劑
Import Information: import

Dates and status

Registration Date: May 15, 2014
Expiry Date: May 15, 2024

About this record

Access comprehensive regulatory information for Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell Virus (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c1795622d8796426ffa2e4f4ff97dde and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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