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"SD" Bioline Influenza Ultra (Non-Sterile) - Taiwan Registration a14d6b776645d2db1650872a2219e23a

Access comprehensive regulatory information for "SD" Bioline Influenza Ultra (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 a14d6b776645d2db1650872a2219e23a and manufactured by STANDARD DIAGNOSTICS, 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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a14d6b776645d2db1650872a2219e23a
Registration Details
Taiwan FDA Registration: a14d6b776645d2db1650872a2219e23a
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Device Details

"SD" Bioline Influenza Ultra (Non-Sterile)
TW: "้€Ÿๅธ" ็™พ่€Œ้ˆๆตๆ„Ÿ็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a14d6b776645d2db1650872a2219e23a

Ministry of Health Medical Device Import No. 015138

DHA09401513807

Company Information

Korea, Republic of

Product Details

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Apr 22, 2015

Jul 28, 2020

Jul 15, 2022

Cancellation Information

Logged out

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