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"Taiyang" Battle Respiratory Virus Screening and Identification Kit (Unsterilized) - Taiwan Registration 6de84a63ecca4ecbf35565451fcd5911

Access comprehensive regulatory information for "Taiyang" Battle Respiratory Virus Screening and Identification 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 6de84a63ecca4ecbf35565451fcd5911 and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is EVERLIGHT BIOTECH(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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6de84a63ecca4ecbf35565451fcd5911
Registration Details
Taiwan FDA Registration: 6de84a63ecca4ecbf35565451fcd5911
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Device Details

"Taiyang" Battle Respiratory Virus Screening and Identification Kit (Unsterilized)
TW: "ๅคชๆš˜" ๅทด็‰น็ˆพ ๅ‘ผๅธ้“็—…ๆฏ’็ฏฉ้ธๅ’Œ้‘‘ๅฎš่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6de84a63ecca4ecbf35565451fcd5911

DHA04401117003

Company Information

Ireland

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 13, 2011

Dec 13, 2021

Aug 15, 2023

Cancellation Information

Logged out

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