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"GHope" Influenza A&B Virus Antigen Rapid Test (Non-Sterile) - Taiwan Registration d76504632b3790e08cff6972ed985ee4

Access comprehensive regulatory information for "GHope" 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 d76504632b3790e08cff6972ed985ee4 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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d76504632b3790e08cff6972ed985ee4
Registration Details
Taiwan FDA Registration: d76504632b3790e08cff6972ed985ee4
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Device Details

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

Registration Details

d76504632b3790e08cff6972ed985ee4

Ministry of Health Medical Device Import No. 015386

DHA09401538600

Company Information

Product Details

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Jun 26, 2015

Jun 26, 2020

May 19, 2022

Cancellation Information

Logged out

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