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"GHope" Adenovirus Antigen Rapid Diagnostic Kit (Non-Sterile) - Taiwan Registration 5846541fdb748dbaa03a27b7488acccb

Access comprehensive regulatory information for "GHope" Adenovirus Antigen Rapid Diagnostic Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5846541fdb748dbaa03a27b7488acccb and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY 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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5846541fdb748dbaa03a27b7488acccb
Registration Details
Taiwan FDA Registration: 5846541fdb748dbaa03a27b7488acccb
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Device Details

"GHope" Adenovirus Antigen Rapid Diagnostic Kit (Non-Sterile)
TW: "็‚ฌๅˆ" ่…บ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

5846541fdb748dbaa03a27b7488acccb

Ministry of Health Medical Device Import No. 013879

DHA09401387900

Company Information

Product Details

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Feb 25, 2014

Feb 25, 2019

May 19, 2022

Cancellation Information

Logged out

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