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"GHope" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile) - Taiwan Registration c57e4f678de6776250a8752be8c5e3ba

Access comprehensive regulatory information for "GHope" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (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 c57e4f678de6776250a8752be8c5e3ba and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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c57e4f678de6776250a8752be8c5e3ba
Registration Details
Taiwan FDA Registration: c57e4f678de6776250a8752be8c5e3ba
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Device Details

"GHope" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile)
TW: "็‚ฌๅˆ"ๅกๅฟ…ๅˆฉๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹่ˆ‡Bๅž‹ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

c57e4f678de6776250a8752be8c5e3ba

Ministry of Health Medical Device Import No. 014243

DHA09401424302

Company Information

Product Details

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Jun 13, 2014

Jun 13, 2019

May 19, 2022

Cancellation Information

Logged out

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