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"ACRO" TB Rapid Test (Non-Sterile) - Taiwan Registration cf9df0c2390d413a294d57bfacdd89ba

Access comprehensive regulatory information for "ACRO" TB 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 cf9df0c2390d413a294d57bfacdd89ba and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD 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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cf9df0c2390d413a294d57bfacdd89ba
Registration Details
Taiwan FDA Registration: cf9df0c2390d413a294d57bfacdd89ba
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Device Details

"ACRO" TB Rapid Test (Non-Sterile)
TW: "่‰พๅฟซ้œฒ" ็ตๆ ธๆกฟ่Œๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

cf9df0c2390d413a294d57bfacdd89ba

Ministry of Health Medical Device Import No. 016994

DHA09401699402

Company Information

United States

Product Details

C Immunology and microbiology devices

C3370 Mycobacterium tuberculosis immunofluorescent reagent

Imported from abroad

Dates and Status

Sep 10, 2016

Sep 10, 2021

Aug 09, 2023

Cancellation Information

Logged out

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