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Abbot's Rotavirus/Adenovirus Rapid Test (Unsterilized) - Taiwan Registration 59157f6987a2353c99a943101039afab

Access comprehensive regulatory information for Abbot's Rotavirus/Adenovirus Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 59157f6987a2353c99a943101039afab and manufactured by ABBOTT DIAGNOSTICS KOREA 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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59157f6987a2353c99a943101039afab
Registration Details
Taiwan FDA Registration: 59157f6987a2353c99a943101039afab
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Device Details

Abbot's Rotavirus/Adenovirus Rapid Test (Unsterilized)
TW: โ€œไบžๅŸนโ€่ผช็‹€็—…ๆฏ’/่…บ็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

59157f6987a2353c99a943101039afab

DHA04400907708

Company Information

Korea, Republic of

Product Details

It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" and "Poliovirus Serum Reagent (C.3405)" of the Classification and Grading Management Measures for Medical Devices.

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3405 ๅฐๅ…’้บป็—บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 12, 2010

Aug 12, 2025