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Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell Virus (Unsterilized) - Taiwan Registration 0c1795622d8796426ffa2e4f4ff97dde

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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0c1795622d8796426ffa2e4f4ff97dde
Registration Details
Taiwan FDA Registration: 0c1795622d8796426ffa2e4f4ff97dde
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Device Details

Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell Virus (Unsterilized)
TW: โ€œ็”Ÿ็ ”โ€ๅฟซ็ดๅจๆต่กŒๆ€งๆ„Ÿๅ†’ๆšจๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0c1795622d8796426ffa2e4f4ff97dde

DHA09401414308

Company Information

Product Details

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.

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

May 15, 2014

May 15, 2024