Pure Global

Thermo Fisher Scientific Respiratory Fusion Viral Antigen Fluorescence Test Kit (Unsterilized) - Taiwan Registration 50662dbb2c1fbc6342e97972d2d54db1

Access comprehensive regulatory information for Thermo Fisher Scientific Respiratory Fusion Viral 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 50662dbb2c1fbc6342e97972d2d54db1 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
50662dbb2c1fbc6342e97972d2d54db1
Registration Details
Taiwan FDA Registration: 50662dbb2c1fbc6342e97972d2d54db1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Thermo Fisher Scientific Respiratory Fusion Viral Antigen Fluorescence Test Kit (Unsterilized)
TW: "่ณฝ้ป˜้ฃ›ไธ–็ˆพ็ง‘ๆŠ€" ๅ‘ผๅธ้“่žๅˆ็—…ๆฏ’ๆŠ—ๅŽŸ่žขๅ…‰ๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

50662dbb2c1fbc6342e97972d2d54db1

DHA09402353401

Company Information

Product Details

It is limited to the first level of identification of the "Respiratory Fusion Cell Virus Serum Reagent (C.3480)" 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‘

Input;; QMS/QSD

Dates and Status

Jul 10, 2024

Jul 10, 2029