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Alere i Influenza A&B - Taiwan Registration 30bff5a3cea5b71721c72d2e2e4205cc

Access comprehensive regulatory information for Alere i Influenza A&B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30bff5a3cea5b71721c72d2e2e4205cc and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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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30bff5a3cea5b71721c72d2e2e4205cc
Registration Details
Taiwan FDA Registration: 30bff5a3cea5b71721c72d2e2e4205cc
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Device Details

Alere i Influenza A&B
TW: ็พŽ่‰พๅˆฉ็ˆพๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’ๆ ธ้…ธๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
MD
Cancelled

Registration Details

30bff5a3cea5b71721c72d2e2e4205cc

Ministry of Health Medical Device Import No. 027999

DHA05602799903

Company Information

United States

Product Details

C Immunology and microbiology devices

C3980 Multi-standard nucleic acid test reagent for respiratory viruses

Imported from abroad

Dates and Status

Dec 16, 2015

Dec 16, 2020

Jul 15, 2022

Cancellation Information

Logged out

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