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"Quick test" pylori rapid test reagent (unsterilized) - Taiwan Registration 4ad90f5d3a8b165ff2135b5378b3b7c4

Access comprehensive regulatory information for "Quick test" pylori 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 4ad90f5d3a8b165ff2135b5378b3b7c4 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. 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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4ad90f5d3a8b165ff2135b5378b3b7c4
Registration Details
Taiwan FDA Registration: 4ad90f5d3a8b165ff2135b5378b3b7c4
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Device Details

"Quick test" pylori rapid test reagent (unsterilized)
TW: "้€Ÿๆธฌ"ๅนฝ้–€ๆกฟ่Œๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4ad90f5d3a8b165ff2135b5378b3b7c4

DHA04401124100

Company Information

Spain

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 28, 2011

Dec 28, 2016

Mar 09, 2017

Cancellation Information

Logged out

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