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"Quick Test" Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized) - Taiwan Registration a14c20bd7f40c69cc62502d1c4e5ce02

Access comprehensive regulatory information for "Quick Test" Respiratory Fusion Cell Virus 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 a14c20bd7f40c69cc62502d1c4e5ce02 and manufactured by CERTEST BIOTEC, S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CERTEST BIOTEC S.L., 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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a14c20bd7f40c69cc62502d1c4e5ce02
Registration Details
Taiwan FDA Registration: a14c20bd7f40c69cc62502d1c4e5ce02
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Device Details

"Quick Test" Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized)
TW: "้€Ÿๆธฌ" ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a14c20bd7f40c69cc62502d1c4e5ce02

DHA09401728007

Company Information

Spain

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 14, 2016

Dec 14, 2021

Mar 15, 2022

Cancellation Information

Logged out

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