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Thermo Fisher Scientific Adenovirus Antigen Fluorescence Test Kit (Unsterilized) - Taiwan Registration bd04fb75bb6448e5d1fd864f5c07c611

Access comprehensive regulatory information for Thermo Fisher Scientific Adenovirus Antigen Fluorescence Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd04fb75bb6448e5d1fd864f5c07c611 and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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bd04fb75bb6448e5d1fd864f5c07c611
Registration Details
Taiwan FDA Registration: bd04fb75bb6448e5d1fd864f5c07c611
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Device Details

Thermo Fisher Scientific Adenovirus Antigen Fluorescence Test Kit (Unsterilized)
TW: "่ณฝ้ป˜้ฃ›ไธ–็ˆพ็ง‘ๆŠ€" ่…บ็—…ๆฏ’ๆŠ—ๅŽŸ่žขๅ…‰ๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

bd04fb75bb6448e5d1fd864f5c07c611

DHA09402348501

Company Information

Product Details

It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" of the Administrative Measures for the Classification and Grading of Medical Devices.

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

May 24, 2024

May 24, 2029