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"ACRO" Flu A&B Rapid Test (Non-Sterile) - Taiwan Registration e9275fee5ef6e5700d71b4fdde4427c2

Access comprehensive regulatory information for "ACRO" Flu A&B 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 e9275fee5ef6e5700d71b4fdde4427c2 and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ACRO BIOTECH. INC., and 1 recent registrations in the same category. 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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e9275fee5ef6e5700d71b4fdde4427c2
Registration Details
Taiwan FDA Registration: e9275fee5ef6e5700d71b4fdde4427c2
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Device Details

"ACRO" Flu A&B Rapid Test (Non-Sterile)
TW: "ๆ„›ๅฏ็พ…" A+Bๅž‹ๆต่กŒๆ€งๆ„Ÿๅ†’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e9275fee5ef6e5700d71b4fdde4427c2

Ministry of Health Medical Device Import No. 017416

DHA09401741606

Company Information

United States

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 devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Jan 16, 2017

Jan 16, 2022

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