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"Abbot" adenovirus antigen rapid test reagent (unsterilized) - Taiwan Registration 4d72344e11118606b70e0eafbc2a8cb0

Access comprehensive regulatory information for "Abbot" adenovirus antigen rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4d72344e11118606b70e0eafbc2a8cb0 and manufactured by ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT. 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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4d72344e11118606b70e0eafbc2a8cb0
Registration Details
Taiwan FDA Registration: 4d72344e11118606b70e0eafbc2a8cb0
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Device Details

"Abbot" adenovirus antigen rapid test reagent (unsterilized)
TW: โ€œไบžๅŸนโ€่…บ็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4d72344e11118606b70e0eafbc2a8cb0

DHA04401128800

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Jan 11, 2012

Jan 11, 2022

Apr 12, 2024

Cancellation Information

Logged out

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